Novartis AG

Job ID REQ-10021623 Oct 03, 2024 Switzerland Summary Develop and validate image analysis algorithms to characterize cellular phenotypes and quantitate molecular targets in high throughput imaging. Design and implement algorithms to refine image quality and robustly isolate and extract desired features. Research and implement novel image and data processing technologies to create effi-cient and reusable solutions, ensuring reproducibility of analytical pipelines. Communicate and present results to a diverse audience of computational and experi-mental scientists. About the Role Requirements : PhD/MS in computer science, biomedical image computing, computational imaging, or a related quantitative field, with 5+ years of relevant experience in industry or academia. Strong programming and data analysis skills in Python. Comfortable working in a Linux HPC environment and skilled in data-parallel processing. Solid understanding of machine and deep learning technologies. Demonstrated background in developing innovative approaches to solve image analysis problems. Strategic ability to identify and select problems where techniques developed in ML/AI can have a significant impact. Experienced in strategically defining and assessing benchmarking and evaluation approaches for ML/AI algorithms, particularly in cases where prior benchmarks may not exist. Enjoy working in a collaborative, multidisciplinary environment and possess a strong willingness to learn from others' expertise in drug discovery. Excellent communication and interpersonal skills to effectively interact with a diverse group of scientists and technical staff. Self-motivated and capable of working in a team environment. Desirable: Working knowledge of imaging platforms across a range of modalities. Skilled in implementing machine/deep learning techniques to solve scientific or engineering problems in the field of life sciences, with a focus on fine-tuning foundational models using major deep learning frameworks (e.g., PyTorch, TensorFlow, JAX) or high-level libraries (e.g., Hugging Face, Lightning). Strong background in computer vision or computational imaging. Demonstrated record of collaborative software development, especially in distributed teams. : Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network : (Use provided wording - do not change) If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Data and Digital Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10021590 Sep 20, 2024 Switzerland Summary As part of the Drug Product Development Scientific Office you should provide strategic and technical guidance on product design and development in liaison When you are a part of the Development team, you'll have countless opportunities to develop your career, as you-ll be surrounded by people you can learn from and help you reach your full potential. Our team is seeking a Drug Development Technologies Strategy Lead. As part of the Drug Product Development Scientific Office you will provide strategic and technical guidance on product design and development in liaison with key stakeholders in CMC, drive engagement with industry consortia and health authorities to enable new technologies implementation, and propose and drive solutions to development challenges. This role is based in Basel, Switzerland. About the Role Your responsibilities include, but are not limited to: Champion holistic understanding of patient- and payer focused drug development and incorporate new technologies (pharmaceutical / in-silico) in conjunction with Health Authorities expectations. Engage in industry consortia to shape regulatory environment and influence key opinion leaders. Liaise with key stakeholders, including Biomedical Research, Global Program Teams, Devices and Primary Packaging, Regulatory CMC, Quality, and Commercial Manufacturing sites, to integrate Drug Product requirements with their needs for a patient-centric product. Provide strategic and technical guidance on Drug Product Design and product development strategy Support / drive interactions with health authorities through participation on briefing packages Proactively identify, lead/propose solution oriented plans to resolve drug product development challenges/barriers. Lead scientific programs and act as member of advisory boards for scientific issues Minimum requirements 10+ years experience in the biopharmaceutical industry with a Scientific qualification. Prior experience in project leadership or people management paired with the ability to engage cross-functional teams Experience of cross-functional collaboration and leading within a matrix? Experience in Drug Product manufacturing of sterile dosage forms including frozen, liquid, and lyophilized formulations in vials and pre-filled syringes Experience in Biologics development, and specifically DP process development, understanding of drug product manufacturing process operations such as mixing, sterile filtration, and aseptic fill/finish. Relevant experience of developing and implementing strategies of patient-centered science related work Analytical thinking to anticipate impact and consequences Experience in writing regulatory modules including INDs and BLAs Knowledge of regulatory guidance from the FDA and EMA for development of biologic drug products Knowledge of USP and Ph. Eur. as it relates to biologics development Learning agility towards new delivery technologies Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture&nbsp ; You-ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No

Job ID REQ-10023201 Sep 30, 2024 Switzerland Summary Location: Basel, Switzerland or London, UK In this role, you will lead, manage and execute IP activities in the Commercial IP team, ensuring the highest quality and successful implementation of patent and regulatory exclusivity litigation strategies for commercial and later-stage development products. About the Role Key Responsibilities: Develop and implement highest quality patent and regulatory exclusivity strategies for commercial and later-stage development products worldwide, including litigations, EPO oppositions, due diligences, and third-party strategies. Lead complex and high-impact patent and regulatory exclusivity litigations for commercial and later-stage development products, including coordination and management of outside counsel, ensuring the use of best litigation practices, and that litigation is of the highest quality, is consistent across the portfolio of matters, and is appropriately reported and budgeted. Build relationships with business partners, and provide clear, informed, and strategic counseling on all aspects of patent and regulatory exclusivity issues relating to commercial and later-stage development products. Role-modeling collaboration, problem solving approaches, and highest-quality litigation strategies. Be a highly contributing member of the Commercial IP team and collaborate with other Novartis IP and legal colleagues to ensure all IP objectives are met. What you-ll bring to the role: Essential Requirements: University degree (B. Sc. or higher) in chemical sciences, biological sciences, chemical engineering or similar European Patent Attorney and/or Law Degree from law school in Europe (including the UK and Switzerland) Extensive experience in IP litigation including pan-European litigation and/or EPO opposition role in pharmaceutical area (private or corporate practice) Proficient in English, additional languages beneficial Industry and/or significant case experience in life sciences Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Legal Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 London (The Westworks), United Kingdom Functional Area Legal & Intellectual Property & Compl. Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10023893 Oct 01, 2024 Switzerland Summary Next Generation Scientist About the Role The Next Generation Scientist Program is an intensive internship program for talented and motivated research scientists from low- and middle-income countries. The 3-month program (01 June to 31 August 2025), hosted at our research site in Basel, Switzerland, is designed to foster both their scientific and professional development and consists of classroom sessions, group work assignments and active individual contribution. Guided by Novartis mentors, the interns work on a jointly agreed upon, pre-competitive scientific or clinical research project. Additionally, they learn about the pharmaceutical drug discovery and development process as well as participate in a leadership development program designed to enhance decision-making and communication skills. The internship program is run jointly by Novartis and the University of Basel. The Next Generation Scientist Program aims to build scientific and leadership capability in low- and middle-income countries by enhancing the skills of local scientists and by facilitating the knowledge transfer to their wider scientific communities upon their return home. An internship is possible in any of the broad range of therapeutic areas in which Novartis is involved; scientists with background and interest in malaria, dengue, cryptosporidiosis, visceral leishmaniasis, leprosy, sickle cell disease or Chagas disease are encouraged to apply. Application : Please make sure to add the following documents to your application, combined in one PDF file : CV or résumé Letter of recommendation/support from a faculty member Letter of motivation how the program will benefit you Research question of interest Current MSc or PhD research proposal Academic transcripts/grade reports Minimum requirements Enrolled at university as MSc, PhD or MD student in a geography of scope (low- and middle-income country) Research background in malaria, dengue, cryptosporidiosis, visceral leishmaniasis, leprosy, sickle cell disease or Chagas disease preferred Active participation in all program and training activities expected Good verbal and written English communication skills Ability to work independently and in groups Good organizational skills Duration and dates: 12-week program from 01 June to 31 August 2025; onsite Basel Campus, Switzerland Preferred field of studies: Natural and Pharmaceutical Sciences, Medicine, and related fields of study Language: English Why Novartis: Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Others Job Type Full time Employment Type Early Talent (Fixed Term) Shift Work No

Job ID REQ-10021326 Sep 30, 2024 Switzerland Summary -Leads the strategic and operational planning and management of the assigned clinical program(s) from an end-to-end clinical operations perspective. The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As CDMD in the Renal TA, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. About the Role Your responsibilities will include, but are not limited to: Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program Leading development of clinical sections of trial and program level regulatory documents Driving execution the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards May work with Biomedical Research/Translational Medical Sciences to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. What you bring to the role: MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification or eligibility in disease area preferred Minimum of 7 years of experience in clinical research or drug development Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required. - 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry required. Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports Demonstrated ability to establish effective scientific partnerships with key stakeholders Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes Previous global people management experience is preferred, though this may include management in a matrix environment. *Final job title and associated responsibilities will be commensurate with the successful candidates- level of expertise (Senior/Director/Associate) Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 Dublin (Novartis Corporate Center (NOCC)), Ireland Alternative Location 2 London (The Westworks), United Kingdom Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10019891 Oct 02, 2024 Switzerland Summary At Novartis, we are reimagining medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. In 2020, we touched 800 million patients with our products. How can we continue to advance our science to help even more patients in need? We believe the answers are found when curious, courageous, and collaborative people are empowered to ask new questions, make bolder decisions, and take smarter risks. In Global Discovery Chemistry (GDC) at the Biomedical Research in Basel, Switzerland, we are at the core of Novartis- purpose, designing and making new molecules for treating patients. We are looking for a highly motivated, passionate researcher with a strong scientific background in biocatalysis, a curious mind-set, and cultural agility to help inventing innovative medicines and advance the frontiers of drug discovery. Join us and help reimagine medicine! Please note this position is written for Associate Director level - however we can hire at Director for those with more established careers with a track record of leadership experience. About the Role Your responsibilities Lead a multidisciplinary team of scientists in a highly collaborative environment to discover and develop novel therapies for high unmet medical needs Evolve scientific strategy for the team and maximize the impact of scientists in your team Work in close collaboration with multiple line functions to enable project success through state-of-the-art biocatalysis approaches including stereoselective synthesis of building blocks and intermediates, metabolite synthesis and late-stage functionalization Lead and complete scientific and technical initiatives by preparing, monitoring, adapting, supporting deployment of novel technologies, and collaborate with internal and external partners around the world Develop and lead global strategic initiatives to shape the future of biocatalysis and its role in drug discovery at BR, as a natural expansion of your sphere of influence and leadership team responsibilities Mentor, coach, and develop a dynamic team of scientists Act as an ambassador of BR to external groups and develop new relationships What you will bring to the role PhD degree in bioorganic chemistry or related life science discipline with profound understanding of biocatalysis and at least 7+ years of industrial experience applying biocatalysis in drug discovery or development settings Significant project and group leadership experience and a track-record of impact on multiple projects. An in depth understanding of applying enzymes to tackle complex synthetic challenges and providing invaluable guidance and solutions to address essential scientific queries to scientists in a broader drug discovery context A mind-set of curiosity and openness to diverse thinking, with an enthusiasm to develop yourself and others Excellent written and verbal communication and strong influencing skills, with an ability to present and discuss project strategies and challenges Strong interest in novel technologies and science trends, such as data science and automation/miniaturization, and their application to drug discovery. Aptitude to work in a fast-paced team-oriented environment, demonstrating collaborative nature and ability to influence in a matrix organization Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10020807 Sep 18, 2024 Switzerland Summary Location: On-site lab based in Basel, Switzerland, #LI-onsite Join our team of 280+ curious minds at Novartis Biologics Research Center, where we work daily to make a difference in patients' lives. At Novartis, we are committed to transforming lives through innovative medical solutions. As an Automation Expert you will be at the forefront of helping to expand expertise in lab automation technologies and techniques. About the Role Our Biologics Center is at the forefront of antibody discovery and development. We are currently seeking an experienced Automation Scientist to help further our expertise in lab automation and progress the science of the department and contribute to our activities and cutting-edge work in antibody discovery and biologics. You will be joining a group of 6 dedicated Lab Automation experts reporting to the Group Lead. Your Responsibilities: Develop, troubleshoot, validate, and run high throughput assays on automated systems for antibody discovery screening campaigns and molecular biology workflows. Plan, run, and troubleshoot processes on automated systems. Assume ownership of assigned automated systems for maintenance, repairs, and readiness state in compliance with internal regulations. Analyse data generated on automated systems using KNIME and capture generated information in data management solutions. Create or modify data analysis workflows for effective flow and data management. Manage projects with internal customers and provide technical support, including creating methods, training users on systems, and supporting them to be self-sufficient with the automation. The role will be highly collaborative, and the successful candidate will demonstrate high attention to detail, innovation and scientific curiosity and have strong communication skills Key Performance Indicators: Successful development and validation of high throughput assays. Timely maintenance and readiness of automated systems. Effective data analysis and management. What You Will Bring to the Role: Bachelor-s/Master-s degree in Biology, Biochemistry, Engineering or equivalent with ideally 5-10 years- experience in the industry, depending on level of qualifications. 5+ years of experience in laboratory automation, preferably in a biologics/antibody discovery environment. Experience with biochemical assay formats such as ELISA and molecular biology work such as plasmid purification. Proven track record in developing processes on Tecan, Beckman-Coulter, Hamilton or other liquid handling platforms, including scheduling software (SAMI, Evoware Plus). Hands-on experience with data management systems such as Genedata Biologics and data analytics platforms or software such as KNIME or Spotfire. Working knowledge or a high level of motivation to use at least one of the following: R, Python, Visual Basic script, or JavaScript. Familiarity with Hamilton systems and Venus Software is highly valued. Strong stakeholder management skills, particularly with internal partners within the department. Ability to undertake good documentation and create SOPs. Ability to assess whether a biological process can be automated and make informed suggestions on the best means to effectively prosecute this. Desirable requirements: Experience with alternative schedulers such as Green Button Go or Cellario An understanding of good data management practices. Experience of configuring/developing API's Experience of SDK (Software Development Kit) to develop custom queries or functions. *Restrictions on working flexibility may apply to this position and can be discussed at interview as required Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<div class="box" id="inserat-details"><h1>Bilingual Childcare is looking for a Montessori daycare Teacher 50-100%</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorie</div><div class="display-field"><a href="/stellenmarkt">Job-/Stellenmarkt</a> › <a href="/lehrerin">KindergärtnerIn/LehrerIn</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 6340 Baar ZG, <a href="/zug">Kanton Zug</a><br/>Obermühle 8 </div></div></div><div class="description">We are a bilingual, private Montessori full-day Kindergarten for children aged 3 months to entering primary school based in Baar. More details on the webpage: <a href="/inserate/122584/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBAILLhlCLR9Wenfp543160Q9SgGE-TJetK-MuL5QVjjP69qGV2SMmTOItKPJm_ttMwMQaN6Fgq6GL9bXetr3Qj0NHf4zSRLM9vS8Nw86ffK9hQfgGfnOvXD3lQYQiILSCY" rel="nofollow" target="_blank">www.montessorizug.ch</a> <br/><br/>Requirements Montessori Teacher 0-3/3-6 and Kindergarten teacher <br/>• Diploma with swiss recognition<br/>• You are native English or German<br/>Montessori degree (or williging to start a training)<br/><br/>You are desiring a long-term employment in a dynamic private institution and you are initiative and willing to take responsibility, resilience, and enjoy working in a team. You are flexible in the interest of the children, parents and the team. You are enjoying conceptual and administrative work.<br/><br/>We offer:<br/>• an exciting and happy work environment, high-quality child care, flexibility in the work schedule, coaching and training "on the job" and regular team meetings, active support for training for long-term staff<br/>• Support from management, teamwork and ownership in the incorporation<br/>• Beautiful, spacious and well-appointed interior and exterior spaces<br/><br/>Are you interested?<br/>Applications with the usual documents (including curriculum vitae, transcripts with grades, certificate of acknowledgment, references, at the time of the earliest possible entry, job requirements etc.)<br/><br/>Montessori Kindergarten of Zug<br/>Obermühle 8<br/>6340 Baar<br/><br/>Mobil: 076 330 47 37<br/>e-mail: <a class="contact-link" data-protected-email="CfDJ8EDJWQJ_AGNPiFWQKPQtWBCLuzSHR3b_gqspAoAiLeUtvR9TwItMbrFSRB0Dj8h8ixJdJYucgW2hx7Udjy2Wp75zEXdcMa_wXX8M5lE0_HFoYx3Rbu1PsVflw7Ia2-eK9woIzHMhVEFji44ZeIzJMxs" href="javascript:;">E-Mail</a></div> <div class="toolbar"><ul><li> Inserat 122584 vom 24.05.2024 </li></ul></div></div></div>

<div class="job_listing-description job-overview col-md-12 col-sm-12"><h2 class="widget-title widget-title--job_listing-top job-overview-title">Overview</h2><h4>Ein Spannungsmesser ist gesucht der Elektriker (m/w/d)</h4><p></p><p>Ein führendes Unternehmen im Bereich der Elektrotechnik, das sich auf Installation, Wartung und Reparatur von elektrischen Systemen und Anlagen spezialisiert hat. Die bedienen sowohl private Haushalte als auch gewerbliche Kunden. Ihr Ziel ist es, durch den Einsatz modernster Technologien und fachmännischer Kompetenz die besten Lösungen anzubieten. Zur Verstärkung des Teams suchen wir einen erfahrenen <strong>Elektriker/In.</strong></p><p><strong>Deine Aufgaben:</strong></p><ul><li>Installation, Wartung und Reparatur von elektrischen Anlagen und Geräten</li><li>Verlegung und Anschluss von Elektroleitungen gemäß den aktuellen Sicherheitsstandards</li><li>Fehlersuche und Fehlerbehebung in elektrischen Systemen</li><li>Durchführung von Elektroinstallationen in Neubauten, Umbauten und Renovationen</li><li>Dokumentation der durchgeführten Arbeiten und Erstellung von Prüfberichten</li><li>Beratung von Kunden bezüglich sicherer und energieeffizienter Elektrolösungen</li></ul><p><strong>Dein Profil:</strong></p><ul><li>Abgeschlossene Ausbildung als Elektriker, Elektroniker für Betriebstechnik oder eine vergleichbare Qualifikation</li><li>Berufserfahrung in der Elektroinstallation</li><li>Gute Kenntnisse der geltenden VDE-Vorschriften</li><li>Selbstständige Arbeitsweise, Zuverlässigkeit und ein hohes Mass an Verantwortungsbewusstsein</li><li>Teamfähigkeit und ausgeprägte Kundenorientierung</li><li>Führerschein der Klasse B</li></ul><p><strong>Wir bieten:</strong></p><ul><li>Eine unbefristete Anstellung in einem zukunftsorientierten Unternehmen</li><li>Attraktive Vergütung und Sozialleistungen</li><li>Weiterbildungs- und Entwicklungsmöglichkeiten</li><li>Moderne Arbeitsausrüstung und ein professionelles Arbeitsumfeld</li><li>Unterstützendes und dynamisches Team</li></ul><p> </p><p>Hast Du Interesse an dieser Anstellung?</p><p>Dann sollten wir uns unbedingt kennenlernen.</p><p>Sende uns Deine vollständigen Bewerbungsunterlagen an Herr Giovanni Porfido.</p></div>

Job ID REQ-10026483 Oct 17, 2024 Switzerland Summary Support the crafting and execution of portfolio strategy and clinical program/functional excellence by actively partnering with the Head of Portfolio Strategy and Operations, Clinical Development Functional Heads, Head of Clinical Workforce Insights, Head of Program Capability and Quality, Head of Advanced Methods and Centers of Excellence, and Head of Data Design and Clinical Innovation. May deputize for Head of Portfolio Strategy and Operations within Clinical Development and with a wide range of cross-functional teams. About the Role Major accountabilities: Undertake diagnostics, study and analysis as required, suggest recommendations and drive resultant actions as approved Continuously looks for new and better ways to deliver CD agenda Prepares content for strategic initiatives on behalf of the Head of Clinical Development/Head Portfolio Strategy & Operations Support the streamlining and provide governance co-leadership for the Head Portfolio Strategy and Operations CD, ensuring consistent messaging across various governance forums (DevLT, CD LT) Support the build of the CD organization, creating and tracking rigorous and quantifiable objectives and communications; to support CD embedding best in class approaches to clinical development while growing deep therapeutic expertise Lead on the benchmarking of CD activities at Novartis vs. peer Key performance indicators: CD KPIs including functional objectives Effective cross-functional collaboration to enable CD led initiatives to strengthen Development objectives Effective crafting and delivery of CD strategic initiatives Optimize the way clinical development delivers the portfolio, including better data quality, shorter timelines to approval, higher phase 3 success rates Minimum Requirements: -5 years people and matrix management required Global people management experience desirable. Strong relationship builder and communicator with experience leading diverse work teams, driving program excellence, engaging functional partners Previous work and leadership in international and multidisciplinary drug development teams Strong knowledge of drug development strategy, Novartis experience in this area is preferred Strong planning and project management skills Organizational awareness, including significant experience working cross-functionally and in global teams. Fluent in English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Alternative Location 1 London (The Westworks), United Kingdom Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<div class="box" id="inserat-details"><h1>Nanny SRK sucht eine Stelle per September 24</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorien</div><div class="display-field"><a href="/stellenmarkt">Job-/Stellenmarkt</a> › <a href="/erzieherin-aushilfe">ErzieherIn/Aushilfe/Springerin</a>, <a href="/nanny">Nanny/Hausangestellte</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 8052 Zürich Seebach, Stadtkreis 11, <a href="/zuerich">Kanton Zürich</a></div></div></div><div class="description">Ich bin 39 Jahre alt, Schweizerin, verheiratet, wohnhaft in 8052 Zürich und eine sehr herzliche, fröhliche und erfahrene Person. Nebst dem Nannylehrgang SRK und Babysitterkurs SRK, habe ich auch den Nothilfekurs für Kleinkinder absolviert. Seit über 14 Jahren arbeite ich nun hauptberuflich als Nanny und suche ab September 2024 eine Stelle für 1- 2 Tag(e) im Raum Zürich.<br/>Montag/ Dienstag/Donnerstag möglich.<br/>Ich freue mich über Ihre Nachricht :-)</div> <div class="pictures"><img alt="Bild 1: Nanny SRK sucht eine Stelle per September 24" src="/inserate/131507/bilder/1"/></div><div class="toolbar"><ul><li> Inserat 131507 vom 20.02.2024 </li></ul></div></div></div>

<p>Wir suchen</p><p></p><ul><li>Wartungs- und Instandhaltungsarbeiten, Störungsbehebungen sowie Ausführung von Reparaturen</li><li>Selbstständige Planung und Koordination der Einsätzein der zugeteilten Region</li><li>Selbstständige Beschaffung von Ersatzteilen</li><li>Kommunikation mit Kunden, Benutzern und technischen Ansprechpersonen</li><li>Periodische Piketteinsätze nach erfolgreicher Pikettzertifizierung</li></ul><p></p><p></p><ul><li>Technische Ausbildung im elektrischen oder mechanischen Bereich</li><li>Berufserfahrung im technischen Bereich, idealerweise im Service-Geschäft</li><li>Gute kommunikative Fähigkeiten sowie Kundenorientierung</li><li>Hohe Eigenverantwortung und Lernbereitschaft sowie eine sicherheitsbewusste und effiziente Arbeitsweise</li><li>Sehr gute Deutschkenntnisse</li><li>Gültiger Fahrausweis (Kat. B)</li></ul><br /><p></p><span style="font-size:11pt;"><span style="font-family:Calibri, sans-serif;">Interessiert? Dann bewerben Sie sich noch heute, gerne auch ohne Motivationsschreiben - wir lernen Sie lieber direkt kennen.<br /><br />Sie haben noch Fragen?<br />Thierry Nufer, gibt unter +41 58 307 35 93 oder über <a href=" E-Mail schreiben ">t</a> E-Mail schreiben gerne Auskunft.</span></span><br /><br />In wenigen Schritten können Sie sich auch direkt auf www.manpower.ch als Gast registrieren und Ihre Bewerbungsunterlagen einreichen

Wir sind eine dynamisch wachsende, international agierende Unternehmensgruppe mit über 100 Jahren Glaserfahrung. 6000 Mitarbeitende in 70 Betrieben machen uns zum grössten glasherstellenden und glasverarbeitenden Familienunternehmen in Europa. Dabei wollen wir<br />gesellschaftlichen Nutzen, Ökologie und Ökonomie stets bestmöglich in Einklang bringen.<br /><br />Die Glas Trösch AG HY-TECH-GLASS in Bützberg zählt innerhalb unserer Gruppe zu den Spezialisten für die Herstellung komplexer Glasprodukte in höchster Qualität. Herzstück des Betriebes ist eine Magnetron-Sputter-Anlage. Mit Plasmabeschichtungen werden ent- und verspiegelte Schichten hergestellt - Glaslösungen für technische Anwendungen und den Automobilbereich<h2><strong>Mitarbeiter/in Spedition und Zuschnitt 100%</strong></h2><h2 class="scheme-headline" >Ihre Aufgaben:</h2><ul> <li>Abwicklung sämtlicher Warenbewegungen (Waren Ein- und Ausgänge, Umlagerungen, etc.)</li> <li>Bewirtschaftung des Lagers</li> <li>Unterstützen und Durchführen von Inventuren</li> <li>Durchführen von Verpackungsarbeiten auf Glasgestelle, Picture-Frames, Container, LKW</li> <li>Transportarbeiten mit Stapler und Krananlagen</li> <li>Mithilfe und Durchführen von Zuschnittaufträgen</li> <li>Bereitstellung von Material für Beschichtung, Spedition und Zuschnitt</li> <li>Unterstützen bei der Opimierung der Arbeitsabläufen und Gesteltung von Hilfsmaterialen</li></ul><h2 class="scheme-headline" >Ihr Profil:</h2><ul> <li>Abgeschlossene Grundausbildung mit Weiterbildung im Logistikbereich</li> <li>Handwerkliches Geschick</li> <li>Von Vorteil sind Führungskompetenz mit hands-on Mentalität</li> <li>Besitz einer Staplerprüfung</li> <li>Gute PC- und MS Office Kenntnisse</li> <li>Selbständige Arbeitsweise und ausgesprochenes Verantwortungsbewusstsein</li> <li>Belastbarkeit, Flexibilität sowie präzises und exaktes Arbeiten</li> <li>ERP-Anwender Kenntnisse</li> <li>Hohe Selbstorganisation erwünscht</li> <li>Gute Deutschkenntnisse in Wort und Schrift</li> <li>Englisch- und Französischkenntnis sind von Vorteil</li></ul><h2 class="scheme-headline" >Wir bieten:</h2><ul> <li>Interessante und anspruchsvolle Tätigkeit</li> <li>Möglichkeit der Weiterentwicklung zu einer Leitungsposition</li> <li>Gründliche Einarbeitung</li> <li>Angenehmes Arbeitsklima in einem leistungsorientierten Team</li> <li>Eintritt nach Vereinbarung</li></ul>Mit Begeisterung schaffen wir Lebensqualität mit dem faszinierenden Werkstoff Glas. Werden Sie ein Teil davon!<br /> <br />Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre vollständige Online-Bewerbung mit Foto

Ausbildung zum Logistiker EFZ (w/m/d)ab August 2025 ; Standort: Sisseln AGDu möchtest einen wertvollen Beitrag für die Gesundheit von Patient*innen leisten? Und eigenverantwortlich etwas wirklich Sinnvolles bewirken? Dann freuen wir uns auf Dich! Excellence beyond manufacturing – dafür stehen wir als Aenova, einer der weltweit führenden Auftragshersteller und -entwickler für die Pharmaindustrie mit 4.000 Mitarbeitenden an 15 Standorten. Unser Standort in Sisseln ist Kompetenzzentrum für komplexe und innovative Solida.Was erwartet Dich?Im Bereich Lager bewirtschaftest Du als Logistiker/in EFZ Güterlager und optimierst deren Nutzung. Du nimmst Güter entgegen, kontrollierst sie und verbuchen die Wareneingänge im Computersystem. Mit Hilfe von Flurförderzeugen lagerst Du die Güter in geeigneter Weise ein oder beladest Fahrzeuge fachgerecht. Ordnung und Sauberkeit werden im Lager grossgeschrieben. Während der 3-jährigen Ausbildung arbeitest Du an verschiedenen Stationen mit und absolvierst unter anderem die Staplerprüfung.Was solltest Du mitbringen?Real-/Sekundarschule erfolgreich abgeschlossenGute Deutschkenntnisse in Wort und Schrift, Englischkenntnisse von VorteilSpass am Lernen von neuen ThemenDu bist speditiv und ausdauernd und kannst Dich gut konzentrierenFreude am praktischen Arbeiten sowie handwerkliches GeschickSelbstständiges, verantwortungsbewusstes und exaktes ArbeitenDu bist teamfähig und verfügst über ein hohes Mass an Engagement und MotivationWas wir bieten:Enge Begleitung der Ausbildung durch Lehrlingsbetreuer und FachpersonenWachstumsorientiertes und dynamisches UmfeldSpannende, auch funktionsübergreifende AufgabenAktive Mitgestaltungsmöglichkeiten im eigenen Bereich Das Werk in Sisseln zeichnet sich aus für das sehr familiäre, unterstützende, freundliche und respektvolle Umfeld mit seinen über 160 Mitarbeitenden

<p>Du liebst süße Köstlichkeiten und hast ein Auge fürs Detail? Werde Teil unseres engagierten Teams und gestalte die leckersten Kreationen mit! Wir bieten dir eine abwechslungsreiche Tätigkeit in einem modernen Umfeld, in dem du deine Fähigkeiten weiterentwickeln kannst.</p><br/><h2>Was Sie bewegen</h2><p><ul><li>Konditorei-Produkte vom Produktionsband abnehmen und in Transportkisten legen</li><li>Bedienen und Einrichten der Etikettiermaschinen</li><li>Probleme erkennen und Störungen beheben, Aushilfe am Band</li><li>Herstellung von Produkten wie Vermicellebecher, Schwarzwäldertorten, Cremeschnitten etc.</li><li>Qualitätskontrollen durchführen und Hygienerichtlinien einhalten</li></ul></p><br/><h2>Was Sie mitbringen</h2><p><ul><li>Abgeschlossene Grund- oder Weiterbildung · von Vorteil als Koch/ Köchin, Konditor in oder Bäcker in</li><li>1-3 Jahre im Berufsleben · von Vorteil in der Lebensmittelproduktion </li><li>Deutsch (gute Kenntnisse) · </li><li>Teamfähigkeit und Zuverlässigkeit</li><li>Genauigkeit und Verantwortungsbewusstsein</li><li>Technisches Verständnis</li></ul></p><br/><h2>Was wir Ihnen bieten</h2><p><ul><li>Sozialleistungen · 730 Tage Krankentaggeld bei vollem Nettolohn<br/></li><li>Cumulus-Punkte · Zusätzliche Cumuluspunkte bei Gütern des täglichen Bedarfs und bei Non-Food/Investitionsgütern</li><li>Mitarbeiterangebote · Mitarbeiterpunkte Cumulus, Vergünstigte Mobileabos, Höhere Zinssätze Migros Bank, Beiträge Klubschule/Fitness und mehr<br/></li><li>Klubschule Migros · Rückerstattung von max. 70% der Kurskosten / CHF 1'000 pro Kurs ohne Jahreslimit<br/></li><li>Du-Kultur · Hoi, hoi zämä, sali - wir sind per Du!<br/></li><li>Entwicklungsmöglichkeiten · Du erhältst die Chance, dich zu entwickeln, und profitierst von der Organisation eines grossen Unternehmens.</li></ul></p><br/><h2>Bewerbung & Kontakt</h2><p>Aline Häny<br/>Recruiterin<br/>0628558204<br/> E-Mail schreiben </p>

JOB PURPOSEResponsible for the maintenance and repair of all the plumbing facilities on board. Assists the Engineers in repairing and maintaining machinery to uphold technical standards demanded by the Company.KEY ACCOUNTABILITIESFollows the instruction of the Hotel Engineer concerning methods and procedures for the maintenance and upkeep of technical plumbing equipment;Repairs, maintains and clean machinery and equipments on board, as requested by the Hotel Engineer;Works always in accordance with acceptable standards, avoiding waste of material and always respecting all injury prevention rules;Ensures the cleanliness and tidiness of the plumbing workshop and tools;Performs any other duty assigned by supervisors or General Manager;Follows and understands the Company environmental policies, rules and regulations.QUALIFICATIONS (skills, competencies, experience)FluentEnglish, oral and written.To be at least 18 years of age and in good health with no physical limitations, including vision;At least 3 years’ experience working in plumbing position or similar;Ability to work long hours under pressure;Good interpersonal skills, positive attitude and willingness to learn;VISA REQUIREMENTS (if any)In the course of our recruitment and selection process, we may make your PersonalInformation available to third parties such as recruitment agency, intermediaries and other businesspartners

Für unsere Abteilung Engineering, suchen wir per sofort oder nach Vereinbarung eine/nIngenieur/in Sekundär- und Leittechnik 80-100%In dieser spannenden Funktion sind Sie für die Planung, Projektierung, Support und Weiterentwicklung von Leit- und Sekundärtechnik über aller Medien zuständig.Das ist Ihr Job Sicherstellen des Anforderungsmanagements der Leittechnik und Leitsysteme, Sekundärtechnik und Automatisierungstechnik über alle Medien Umsetzung der Schnittstellen zum Datenaustausch zwischen den internen und externen Systemen (u.a. BKW, SEGA, BSG, usw.) gemäss OT/IT-Konzept, und Data-Engineering zur Anbindung von neuen Anlagen an die Betriebsführung Projektleitung für Investitionsprojekte der OT und Sekundärtechnik mit Gesamtverantwortung für Kosten, Termine, Qualität und Resultate Sicherstellen des Nachführungsprozesses der Dokumentation für die Sekundärtechnik, Schutzeinstellungen und punktuell für die OT-Systeme Gesamtverantwortung für den Schutz im elektrischen Netz (Schutzkonzepte, Lifecycle Management für Schutzgeräte, Engineering, Parametrierung, Wartung) und für die Aufbau und Pflege der langfristigen Umgebung für embedded Software der gesamten dezentralen Leit- und SekundärtechnikDas bringen Sie mit Elektrotechnische Grundausbildung und Hochschulabschluss FH mit Vertiefung Elektro- oder Energietechnik - Betriebswirtschaftliche Weiterbildung und/oder Projektleiterausbildung von Vorteil Ausgewiesene Berufserfahrung, vorzugsweise im Bereich Sekundärtechnik, Leittechnik und Leitsysteme für die Energieversorgung Sehr gute Erfahrung mit der Programmierung von SCADA-Systemen, Fernwirkgeräten, SPS und Schutzgeräten Hohe IT/OT-Affinität und versierter Umgang mit MS-Office Anwendungen und GIS-Systemen Hauptsprache Deutsch oder Französisch mit guten Kenntnissen der anderen SpracheDas bieten wir Ihnen - unter anderem Transparente Lohnpolitik Vorteilhafte Anstellungsbedingungen Ein starkes Team mit familiärem Umgang* Förderung Ihrer beruflichen EntwicklungWeitere Informationen zum ESB als Arbeitgeber finden Sie hier.Energie Service Biel/BienneWir sind der führende Energiedienstleister und Wasserversorger in der Region Biel. Unser Können und Wissen setzen wir wirkungsvoll und fokussiert für unsere Kundinnen und Kunden ein. Wir setzen auf nachhaltige Energieproduktion sowie Energieeffizienz und gestalten so aktiv die Energiezukunft. Gemeinsam mit Ihnen möchten wir uns weiterentwickeln. Wir bieten unseren Mitarbeitenden attraktive Anstellungsbedingungen, wir unterstützen Sie bei Ihrer Tätigkeit und fördern Ihre berufliche Entwicklung

<h3>BECOME A PART OF THE OMNIA EXPERIENCE!</h3><p>Im THE OMNIA stehen alle Zeichen auf <em>Neustart</em>: Im Juni 2024 ist unsere Mountain Lodge nicht nur in die nächste Saison gestartet, sondern hat mit André Kneubühler als Executive Chef auch eine neue kulinarische Ära eingeläutet!<br /><br /> Wir suchen ein frisch zusammengestelltes Küchenteam, das sich hochmotiviert unserem gemeinsamen Ziel verschreibt, die Qualität unserer Küche zu steigern und dem kulinarischen Angebot des THE OMNIA seine eigene exklusive Note zu verleihen.<br /><br /> Wenn Sie Ihren Beruf lieben, vor Kreativität sprühen und auch mit eigenen Ideen unser süsses Menü bereichern möchten, laden wir Sie herzlich ein, sich als<br /><br /><strong>Chef de Partie Entremetier</strong><br /><br /> bei uns zu bewerben.</p><h3>PROFIL</h3><ul><li>Abgeschlossene Berufslehre (EFZ) und Berufserfahrung als Koch</li> <li>Gute Deutschkentnisse (Englisch von Vorteil)</li> <li>Strukturierte Arbeitsweise und ein hohes Mass an Belastbarkeit</li> <li>Kreative Persönlichkeit mit dienstleistungsorientierter Grundhaltung</li> <li>Zuverlässigkeit, Engagement und Teamspirit</li> <li>Sicheres und kompetentes Auftreten</li> </ul><h3>AUFGABEN</h3><ul><li>Eigenständige Führung und Verantwortung des Postens Entremetier</li> <li>Sicherstellung der konstant hohen Qualität der Speisen</li> <li>Sauberkeits- und Ordnungskontrollen</li> <li>Einhaltung der Qualitätsstandards</li> <li>Mitverantwortung bei der Umsetzung und Überwachung des Hygienekonzeptes</li> </ul><h3>IHRE PERSÖNLICHE THE OMNIA EXPERIENCE</h3><p>Es erwartet Sie eine abwechslungsreiche und verantwortungsvolle Aufgabe in einem jungen und motivierten Team und in einem der besten Hotels der Schweiz. Ein angenehmes und menschliches Arbeitsklima ist uns ebenso wichtig wie eine gesunde Unternehmenskultur. Daher bietet Ihr Arbeitsplatz Ihrer Persönlichkeit sowie Ihren eigenen Ideen reichlich Raum, sich kontinuierlich weiterzuentwickeln.</p> <p> </p> <p>Zermatt - das Dorf mit Weltruf - bietet unzählige Möglichkeiten für eine erlebnisreiche Zeit inmitten der Schweizer Alpen. Zudem profitieren Sie in THE OMNIA von weitern Vorteilen, darunter:</p> <p> </p> <ul><li>eine positionsgerechte Entlöhnung</li> <li>eine Ganzjahresanstellung</li> <li>eine Mitarbeiterunterkunft in Zermatt und zu fairen Konditionen</li> <li>Sprachkurse in Französisch, Deutsch und Englisch</li> <li>eine umfassende Schulung und Crosstrainings beim Eintritt</li> <li>regelmässige Mitarbeiterschulungen und professionelle Trainings</li> <li>ein einzigartiger Arbeitsplatz mit hochwertigen Arbeitsmaterialien und zeitlosen Designklassikern</li> <li>Uniformen vom hauseigenen Designer</li> <li>die Mitgliedschaft bei der Swibeco Vorteils-Plattform mit Vergünstigungen bei unzähligen Dienstleistern</li> <li>die Zermatt Staffcard mit Zugang zu attraktiven Angeboten in Zermatt</li> <li>Family & Friends Rabatt: Familie und Freunde übernachten vergünstigt</li> <li>jede Saison eine Einladung für unsere Mountain Lodge Experience inkl. Weinbegleitung</li> <li>Mitarbeiterfeste, Weihnachtsgeschenke und weitere Aufmerksamkeiten übers Jahr</li> </ul>

<div>Unser Partner ist ein führendes Unternehmen im Bereich der Unternehmensberatung und IT-Lösungen. Welches Unternehmen weltweit dabei unterstützt, ihre Geschäftsprozesse zu optimieren und ihre digitalen Transformationen erfolgreich umzusetzen.<br /></div><br><ul><li>Ausbau des SAP HCM-Teams mit der Option auf Übernahme der Teamleitung</li><li>Federführung in Sales und Presales im Bereich HCM</li><li>Beratung unserer Kunden in SAP-HCM Themen (remote oder vor Ort) – von der Aufnahme der Anforderung, Konzeption der Lösung bis hin zur Umsetzung (inkl. Customizing) und Betrieb der Lösungen</li><li>Leiten von Projekten und Teilprojekten</li><li>Ausbilden von Junior Consultants</li></ul><br><ul><li>Bachelor-Abschluss in Informatik, Wirtschaftsinformatik oder einem verwandten Bereich</li><li>Mindestens 8 Jahre Projekterfahrung in SAP PY oder PT inkl. Customizing</li><li>Fundierte Kenntnisse in in HR-Themen und Prozessen</li><li>Erfahrung im SAP HCM Umfeld</li><li>Starke Problemlösungsfähigkeiten und die Fähigkeit, in einem dynamischen Umfeld zu arbeiten</li><li>Ausgezeichnete Kommunikations- und Beratungsfähigkeiten in Deutsch und Englisch</li><li><div>Erfahrung in der Beratung</div></li></ul><p><br /></p><h2>Benefits<br /><br /></h2><ul><li>Eine herausfordernde und abwechslungsreiche Tätigkeit in einem internationalen Umfeld</li><li>Attraktive Vergütung und Benefits, einschließlich Weiterbildungsmöglichkeiten</li><li>Die Möglichkeit, Ihre Fähigkeiten und Erfahrungen in einem innovativen Unternehmen einzubringen und weiterzuentwickeln</li></ul><p><br /></p><h4>Wir freuen uns auf Ihre Bewerbung.</h4><h4>Für weitere Informationen steht Ihnen Azir Spahiu gerne zur Verfügung.<br /></h4><p><br />Azir Spahiu<br />Senior Consultant<br /><br />T 044 210 40 20<br />M 076 424 28 82<br />E E-Mail schreiben <br /><br />Albedis AG<br />Zähringerstrasse 51<br />8001 Zürich<br /><br /></p>

<span class="jobdescription"><div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:0.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px">Description</h2> </div><div><p style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Motivé∙e par un apprentissage de Mécanicien∙ne de production ? Prêt∙e à devenir une référence dans votre métier grâce à une formation de qualité dans une entreprise leader ? <br/>Rejoignez-nous !</span></span></p><p style="text-align:justify"> </p><p style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Le/La mécanicien∙ne de production fabrique des pièces de laide de machines traditionnelles et à commandes numériques. <br/>Il/Elle interprète des dessins techniques, prépare les outils et les matériels nécessaires à la fabrication des pièces. Il/Elle est chargé∙e du réglage ainsi que du contrôle des machines et est responsable de la qualité des pièces qu’il/elle produit.</span></span></p><p style="text-align:justify"> </p><p style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Cet apprentissage convient à des jeunes gens qui s’intéressent au travail du métal, aux machines industrielles et qui aiment la précision.</span></span></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><i>Profil</i></h2> </div><div><ul><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Bonne représentation spatiale</span></span></li><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Esprit logique et méthodique</span></span></li><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Habileté manuelle et précision</span></span></li></ul></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:0.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px">Pour postuler</h2> </div><div><p style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Si vous êtes motivé∙e à relever le défi, n’hésitez pas à postuler. Votre dossier devra contenir :</span></span></p><ul><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">un curriculum vitae</span></span></li><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">une lettre de motivation</span></span></li><li style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">vos bulletins des trois dernières années scolaires</span></span></li></ul><p style="text-align:justify"> </p><p style="text-align:justify"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Encadré∙e par des formateur∙trice∙s expérimenté∙e∙s, vous pourrez évoluer dans un environnement de travail hors du commun. Cette formation vous assurera d’excellentes perspectives. </span></span><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">Rolex s’engage à vous offrir bien plus qu'un apprentissage : une véritable opportunité de développement personnel et professionnel.</span></span></p><p><span style="color:#ffffff"><span style="font-size:12.0px"><span style="font-family:Arial, Helvetica, sans-serif">#LI-DNI</span></span></span></p></div></div></div></span>

Job ID REQ-10026201 Oct 15, 2024 Switzerland Summary We are offering two 6-months legal trainee position to support the Novartis Operations Legal department on a wide range of legal matters and projects in areas such as contract law, commercial law, M&A and licensing transactions, restructuring, antitrust law etc. About the Role We are offering two 6-months legal trainee position to support the Novartis Operations Legal department on a wide range of legal matters and projects in areas such as contract law, commercial law, M&A and licensing transactions, restructuring, antitrust law etc. Our legal trainee positions offer excellent opportunities to gain first-class, hands-on in-house legal experience within the stimulating, multinational environment of a leading pharmaceutical company. Start dates: January 1, 2025 and June 1, 2025 Duration: 6 months Your responsibilities include: Support M&A and corporate projects, manufacturing and supply agreements, real estate projects, portfolio and manufacturing site divestments, including conducting due diligence, managing data rooms and enquiries in the sale process, and legal project management Support a diverse range of commercial matters relating to the development, procurement, manufacturing, quality assurance and supply chain and distribution of pharmaceutical products Support diverse range of legal department projects, e.g. contract templates, legal trainings, global legal research projects, digitalization, outsourcing etc. Assist in drafting, negotiation and review of a variety of transactional, commercial and technical agreements Draft legal memoranda on a wide variety of legal issues and disputes Provide legal advice to internal clients, draft documents and key position summaries Interact with Novartis global, regional and country legal network What you-ll bring to the role: Education: Swiss Law degree (BLaw plus MLaw or equivalent) Languages: Business-level English (written and spoken); German ideally and additional languages are a plus Experience/Professional requirements: o Prior legal professional experience in a law firm, court or legal in-house department (internships etc.) would be helpful. We are also open to applicants without prior experience who have a strong interest and are motivated to learn on the job o Overall high motivation and ability to work independently Desirable requirements: Other professional experience in the corporate environment is a plus Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com, and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Operations Business Unit CTS Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Others Job Type Full time Employment Type Early Talent (Fixed Term) Shift Work No

Job ID REQ-10023685 Oct 02, 2024 Switzerland Summary Basel, Switzerland Full time. Onsite. #LI-onsite Our Lab Solutions and Scientific Services teams, situated within our Scientific Operations in Biomedical Research, is responsible for providing integrated programs and services that support our scientific community. The team is critical in the mission to enable the Novartis Biomedical Research-s scientists to focus on scientific breakthroughs for patients through data drive, sustainable operational excellence and innovation. About the Role We are now seeking a motivated and experienced Lab Equipment Operations (LEO) Specialist to join our Lab Solutions and Scientific Services team. As a Lab Equipment Operations Specialist, you will be responsible for overseeing the daily operations and logistics of the Lab Equipment Management Program and act as the primary on-site contact for lab equipment inquiries and oversee equipment repair work orders. Additionally, you will oversee the delivery and logistics of surplus lab equipment and assist with onsite activities related to equipment relocation and equipment utilization and sharing initiatives. The LEO specialist spends a substantial part of the time in the laboratories supporting and interacting with customers. Your responsibilities will include: Acting as the accessible contact person in the laboratory: Plan and execute weekly lab tours including interactions with scientists based on lab equipment management inquiries and needs Site Lab Equipment Management (LEM) Program Operations: Deputy to LEO Manager for the daily operations and logistics of the Site LEM Program as the primary liaison for Disease Areas/Functional Areas regarding lab equipment inquiries and supervise the governance of Universal Lab Supply (ULS) work orders within the review framework. Surplus Equipment Logistics: Efficiently coordinate the distribution and logistics of surplus lab equipment with internal and external partners. Communicate with labs for internal sharing opportunities, and drive process improvements. Equipment Sharing Initiatives: Support coordination of equipment sharing initiatives, working closely with scientists and LEM team to identify suitable equipment for sharing. Coordinate with Facilities to support lab equipment logistics: Partner with Novartis campus office teams & campus labs to support lab equipment relocation logistics for lab moves and equipment phase out. Execute onsite tasks for equipment utilization efforts: Carry out the hardware setup, deployment and support the troubleshooting of smart capture and plug load monitors with internal and external stakeholders throughout the site. Support Asset Count Cycle: Update Asset inventory (I.AM) by incorporating relevant information from ULS data sources. Minimum requirements: What you will bring to the role Technical qualification such as Laboratory Technician, or Bachelor-s/Master-s degree or equivalent in a scientific discipline with ideally minimum 3-5 years- experience in a relevant field within Drug Discovery or related area Background in lab operations, good organizational skills, and the ability to collaborate with various stakeholders to ensure smooth and efficient lab functioning. Experience as a lab associate preferred. A person of action, proactive, with effective communication skills, and the ability to make informed decisions. Ability to-prioritize and juggle multiple tasks-simultaneously in a fast-paced environment. Proficiency in-IT tools is required, along with the capacity to quickly learn and master internal processes. Strong understanding of the processes and protocols required in a scientific research organization. Broad knowledge of discipline, methods and technologies Advanced written and spoken English. German language skills an advantage *Restrictions on flexible working arrangements may apply and will be discussed at interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regulär Shift Work No

Job ID REQ-10008420 Oct 16, 2024 Switzerland Summary Location: Basel, Switzerland - Hybrid; United Kingdom - Remote. Closing date for applications: 30th October 2024 About the role: We are seeking an Executive Director to lead a team in the role of Therapy Area (TA) Communications & Patient Advocacy. We are looking for a highly motivated individual who is passionate about making a difference in the lives of patients and who possesses strong communication and advocacy skills. This is an exciting opportunity to lead and shape the strategic direction of a TA Communications & Patient Advocacy team. This role will lead, mentor and develop 7-8 direct reports. About the Role Key Responsibilities: Develop, drive and implement therapy area and product communications and patient advocacy strategy focused on priority pre-launch, launch and in market brands. Development and co-creation of communication and patient advocacy strategies, KPIs and measurement with Germany, China, Japan and advising on strategy, tracking implementation and performance management of product brand strategy to other top-11 markets. Ensure systemic implementation of strategic framework and Analytics & Insights measures to consistently monitor TA and predict performance management above country and for Top 11 market, in alignment with Corporate Affairs Strategy and Operations and with Public Affairs. Establish strategic and ongoing relationships with internal and external partners, leading to business-aligned, long-term collaborations that are valued by and valuable for key audiences, most importantly, patients. Implement launch excellence in line with commercial organization and embed communications and patient advocacy programs in launch readiness plans for priority brands. Represent function on respective leadership team and become trusted strategic business partner to Therapy Area Head. Support talent management and growth for International TA Communications & Patient Advocacy team members. Accountability for securing budget and budget management of respective TA communications and patient advocacy strategies by Commercial and Corporate Affairs teams. Including governance and compliance of Patient Advocacy grants, sponsorships and TOV reporting, supported by the Patient Advocacy governance lead. Lead media relations strategy and implementation, including relationships with media stakeholders, TA/product brand issues and crisis management for respective TA in coordination with Corporate Media Relations. Lead and implement PESO and influencer engagement strategy for respective TA in partnership with top-11 countries. Implement internal communications for key brand milestones and launch activities in coordination with the Executive Director President Corporate Affairs. Essential Requirements: Bachelor-s degree or equivalent experience. Extensive years- experience in diversified communications and patient advocacy with patient relations, leadership and influencing. Demonstrated experience across multiple therapeutic areas. Leading large and/or diverse multi-functional teams with proven ability to cultivate impact. Exemplifies and drives a predictive modelling approach; seeks multidirectional insights to understand our environments and customers, and embraces iterative, measurable experimentation and action. Evidence of using data and insights to drive strategic decision leading to impact on the busi8ness objectives. Business and organisational awareness, enterprise perspective. Product PR communications, social media strategy and implementation Corporate communications, IR, media relations, stakeholder relations, policy. Crisis, issues and agency management. Benefits and rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Commitment to Diversity & Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in any order to receive more detailed information about essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Corporate Affairs Business Unit CTS Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 Home Worker, United Kingdom Functional Area Communications & Public Affairs Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10023916 Oct 14, 2024 Switzerland Summary Location: Basel, Switzerland, or Cambridge, MASS, US Lab Solutions & Scientific Services, situated within the Scientific Operations (SO) organization, is responsible for providing integrated programs and services that support our scientific community, and has a mission to enable the Novartis BioMedical Research-s (BR) lab scientists to focus on science in the lab through data-driven, sustainable operational excellence and innovation. Lab Solutions & Scientific Services consists of four global sub-functions and this role provides global leadership working in the key area of lab equipment management. We are now seeking an experienced Lab asset management expert , preferably with a strong Automation background, to join us as a key member of the global Lab Equipment Management (LEM) program team. About the Role You will ensure the success of the end-to-end lab equipment management program by building strong partnerships with the local operations community, the Asset Strategy Governance Board (ASGB), equipment category SMEs, and other Biomedical Research stakeholders and support functions. Specifically, you will manage the Biomedical Research LEM program end-to-end within your category, including interactions with engaged third parties and support from the local Lab Equipment Operations team. Responsibilities include: Coordinate and chair the global Asset Strategy Governance Board (ASGB) within your category. Develop a global equipment life cycle strategy within your category, collaborating with ASGB, SMEs, Disease Area/Finance Area operations, data analyst, lab equipment operations, procurement, and vendors. Regularly update and maintain the plan based on shifting priorities and changes. Document and maintain life cycle plans, ASGB decisions and guidance documents on Biomedical Research standards within your category, using standard templates within the LEM program. Report key LEM program performance indicators regularly Review and align equipment demand requests with the global strategy within your category, identifying opportunities for bundling and aligning priorities with finance across categories. Align with internal stakeholders on vendor negotiations for CapEx, global service contracts, and consumables with key vendors within your category. Prepare for Capital Acquisition Request (CAR) review at the Investment Review Meeting (IRM) for equipment with an overall strategy and life cycle plan and communicate approvals back to DAs/FAs. Coordinate bundled sourcing across Biomedical Research with involved DAs/FAs. Collaborate closely with finance to manage the budget for the equipment category based on global strategies and forecasting. Minimum Requirements - What you will bring to the role Bachelors, Masters or equivalent in relevant scientific discipline with appropriate years of industry experience in a relevant field within drug discovery or related area. Proven experience in enterprise strategic planning and asset management. Strong technical skills and experience in the equipment category Excellent vendor relations management and negotiation skills Strong leadership skills and the ability to work cross-functionally with various teams and stakeholders. Ability to influence without authority and actively manage key stakeholders Project Management experience and Lean and Six Sigma experience a plus Ability to exercise independent discretion and judgment to solve problems as well as an ability to prioritize effectively in a fast-paced and dynamic environment. Strong understanding of the processes and protocols required in a scientific research organization. Proficiency in using IT tools to capture, manage and analyze data required (e.g. MS Excel, SharePoint & Access, Spotfire, SAP) Excellent communication skills with ability to present information to operations leadership and scientific customers (fluent English with German language considered an advantage) Demonstrated problem-solving and analytical skills and recommend process changes when appropriate Solution-oriented individual with a proven track record of problem solving Broad knowledge of discipline, methods and technologies *Restrictions on flexible working arrangements may apply and will be discussed at interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<p>Gesucht: Dipl. Physiotherapeut / Physiotherapeutin im Kanton Zürich (80%-100%) – Unser Kunde sucht nach einer / einem Physiotherapeutin / Physiotherapeut, die /der das Team auf individuelle Art komplettiert und sich den verschiedenen Herausforderungen des Berufs kompetent stellt.</p><p>Unser Kunde sucht per Juli 2024 Unterstützung in der Domizilbehandlung der Patienten. Die Patienten sind fast ausschliesslich aus dem geriatrischen Bereich. Die Diagnosen/Behandlungsbereiche sind dabei aber sehr vielfältig über alle Bereiche verteilt. Einer der Hauptbereiche sind muskuloskelettale Probleme mit dem Ziel die allgemeine Mobilität wieder zu verbessern.</p><p>Wir laden dich ein, unser Portal zu nutzen und durchzustarten</p><h1><strong>Worauf Sie sich freuen dürfen:</strong></h1><ul><li>Einen festen Arbeitsvertrag</li><li>Überdurchschnittliches Gehalt + Bonus</li><li>Diverse Fort- und Weiterbildungsmöglichkeiten</li><li>Support durch den Arbeitgeber, eine Sekretärin unterstützt das Team und nimmt viele Aufgaben und Arbeiten ab- so kannst du dich vollkommen auf die Therapien konzentrieren</li><li>Dynamisches Team von 8 Kollegen aus Deutschland, Polen, Niederlande und der Schweiz</li><li>Abwechslungsreiche und verantwortungsvolle Tätigkeit</li></ul><p> </p><h1><strong>Ihre Aufgaben als Physiotherapeut in Zürich:</strong></h1><ul><li>Behandlungen von Patienten im Domizilbereich im Einsatzgebiet rund um Zürich</li><li>Dienstfahrzeug wird gerne zur Verfügung gestellt, man ist den ganzen Tag unterwegs und besucht Patienten bei ihnen zu Hause oder in Alters- und Pflegeheimen</li><li>Präventive, diagnostische und therapeutische Massnahmen</li><li>Elektronische Dokumentation</li></ul><p> </p><h1><strong>Ihr Profil als Physiotherapeut in Zürich:</strong></h1><ul><li>Eine abgeschlossene Ausbildung zur/zum Physiotherapeut/ Physiotherapeutin</li><li>Eine selbstständige Arbeitsweise</li><li>Belastbare und flexible Persönlichkeit</li><li>Einfühlsam</li><li>Gute Deutschkenntnisse in Wort und Schrift (B2/ C1)</li><li>Anerkennung SRK oder Precheck positiv</li></ul><p> </p><p>Die Koraal AG ist seit über 10 Jahren darauf spezialisiert, medizinisches Fachpersonal an ausgewählte Arbeitgeber im In- und Ausland zu vermitteln.</p><p> </p>

<div class="box" id="inserat-details"><h1>Spielgruppe Muulwürfli in 8645 Rapperswil-Jona</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorie</div><div class="display-field"><a href="/kinderbetreuung">Kinderbetreuung</a> › <a href="/spielgruppen">Spiel-/Waldspielgruppe</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 8645 Jona, <a href="/st-gallen">Kanton St. Gallen</a><br/>Blumenaustrasse 25 </div></div></div><div class="description">Der Verein Spielgruppe Muulwürfli…… <br/><br/>...bietet ein vielfältiges Angebot für Kinder vor dem Kindergarteneintritt. Wir verfügen über einen grosszügigen, hellen Raum mit genügend Platz zum Spielen und Kind sein. Ein Spielplatz befindet sich ganz in der Nähe.Ebenso gehört ein kleiner Garten, eine Malwand und eine Werk- und Experimentier-ecke zur Einrichtung.<br/><br/>Wir nehmen jedes Kind, wie es ist. Speziellen Gegebenheiten oder besonderen Bedürfnissen begegnen wir unvoreingenommen und offen!<br/><br/>Unsere Leiterinnen sind alles ausgebildete Fachfrauen und Mütter. Regelmässige Weiterbildung ist selbstverständlich. Wertvolle Erfahrungen im Beruf und zu Hause bringen viel Verständnis und Geduld für die bereichernde Arbeit mit Kindern mit. Die Spielgruppenleiterin wird von einer Assistentin unterstützt.<br/>Zudem erfüllen wir das Qualitätslabel des SSLVs.<br/><br/>Der Austausch und die Zusammenarbeit mit den Eltern ist uns wichtig, und bildet das Fundament für eine spannende,erlebnisreiche und glückliche Spielgruppenzeit für Ihre Kinder.<br/><br/>weitere Infos auf unserer Homepage: <a href="/inserate/120625/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBDCTlZwRk7QKTAXz88mqy32pAqT0Oq6p1h0tZf_6sk-gaOktPX5zCRTZuOmrddaw2TAvySkOMfuojZGykEuq4Cyoer97y4BssoMpoZfznlZsVIxPcQpyoDgnQPaws89EmM" rel="nofollow" target="_blank">www.muulwuerfli.ch</a><br/><br/>Wir freuen uns auf viele neugierige Kinder:)</div> <div class="pictures"><img alt="Bild 1: Spielgruppe Muulwürfli in 8645 Rapperswil-Jona" src="/inserate/120625/bilder/1"/></div><div class="toolbar"><ul><li> Inserat 120625 vom 05.10.2024 </li></ul></div></div></div>

Do you have experience in Non-Product Software and Computerized Systems Validation? Are you available for a contract opportunity imminently? If this sounds like you and you are driven by purpose, Join the SOPHiA GENETICS Quality Team as a Quality Engineer, and enable us to make a positive impact on the outcomes for cancer and rare disease patients worldwide. This is a contract opportunity until March 2025, with scope for extension or permanent opportunity. Due to the nature of this role, you can expect to be in our office for a majority of the time connected to our site in Rolle, CH. Our MissionWe believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis. You will have direct input to our mission to democratize data-driven medicine for the ultimate benefit of cancer and rare disease patients across the globe. Your MissionAs part of our quality team, this project focuses on ensuring all software used in design, manufacturing, and quality management processes comply with ISO 13485 standards in accordance with pre-defined process, procedures and templates.The value you bring: Assist in gathering software validation documentation Support the creation or update of software validation plans and protocols Perform verification and validation activities for selected Non-Product Systems and Document Non-Product Systems deliverables and ensure traceability Assist in maintaining a central repository for validation records Prepare documentation and keep records RequirementsTo be best set for success, we see you bringing: Knowledge of software development lifecycle (SDLC) and software validation processes Experience mapping and documenting Non-Product Software or Computerised Systems Validation, ideally within a quality function Basic knowledge of programming or scripting languages (e.g., Python, Java, or others) is a plus Knowledge of quality management standards (ISO 13485, FDA QSR). As an international organization, English is our primary business language and you will need to be fluent (both written and spoken) to progress. As part of your recruitment journey, you should expect to meet English-only speakers. For best chances of success, you should include your CV in English. Unfortunately, non-English CVs have a high likelihood of being rejected at application stage.BenefitsYou will be joining an organisation with the patient at the heart of every decision and action, driven by purpose as we pursue exponential growth. Business recognition and accolades include: Worlds smartest companies (Top 50) 100 Best Places to Work in Boston Top 10 European Tech Startup Top 10 European biotechs startup to watch Top 25 East-Coast Biotech to watch Our benefits package is comprehensive, but varies internationally in-line with local standards and laws. You can discuss a full breakdown with us, but as a brief overview: Sickness and Accident coverage through Helsana Meal Vouchers at 90CHF PM with our partner cafeteria 25 days vacation Voluntary benefits including Fitness and Bank Partnerships A fun and engaging work environment, with Rest & Entertainment space, full stocked free coffee machine and free fruit. Free parking in an easy to access location Our DNALike the strands of DNA itself, SOPHiA GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient & Nimble and Fearlessly Adventurous Our VirtuesAt SOPHiA GENETICS we established our 7 Virtues to clarify how our principles show up each day through action. We decide; We do; We Collaborate; We Innovate; We Empower; We Adapt and We Learn.At the centre of our Virtues is our Mantra, We Care, which provides a constant reminder of the compassionate, benevolent, and hopeful nature of our mission and how it should be threaded through each of our Virtues and everything we do. Learn more about our DNA and Virtues on our Careers portal The Process We use the power of AI to help our partners make decisions. If you’re utilising AI in your search and application process, why not use some of these prompts: ‘What impact can I expect to have on the world by working at SOPHiA GENETICS?’‘I have an interview with SOPHiA GENETICS. What should I know before I meet with them?’‘I am a job title - What can SOPHiA GENETICS offer my career?’ Apply now with your CV and any supporting information. Suitably qualified candidates will be invited through an interview and screening process where you will speak with members of our Talent Acquisition Team, the hiring leader alongside key colleagues and stakeholders from across the business. If you need additional support for accessibility, please contact our TA team for assistance. We appreciate the value external partners can bring, but we operate a direct-hiring model and we are not looking to utilise agency support at this time. All hiring is controlled by Talent Acquisition, potential partners should liaise through TA and not our hiring teams please. Starting Date: ASAP Location: Rolle, CHContract: Temporary Contract – Until March 2025 (Scope for extension/permanent)

Job ID REQ-10009496 Sep 26, 2024 Switzerland Summary Interessierst Du Dich für eine Karriere in einem in-house Rechtsdepartment in einer multinatonalen Pharmafirma? Wir bieten ein spannendes 6-monatiges juristisches Volontariat vom 1. Juni 2025 bis zum 30. November 2025 an. About the Role Interessierst Du Dich für eine Karriere im Rechtsbereich? Wir haben die perfekte Gelegenheit für Dich! Unsere Position als juristische/-r Volontär/-in (Legal Trainee) bietet Dir hervorragende praktische Erfahrung im Inhouse-Bereich innerhalb der dynamischen und multinationalen Umgebung eines führenden Pharmaunternehmens. Mehr als 70'000 einzigartige Individuen arbeiten bei Novartis, alle mit unterschiedlichen Bedürfnissen und Bestrebungen, vereint durch ein inspiriertes Ziel: die Medizin für Millionen von Patienten und Patientinnen weltweit neu zu denken. Wir suchen eine/-n motivierte/-n Legal Trainee, der/die die Neugier mitbringt, sich interessanten und herausfordernden neuen rechtlichen Fragenstellungen zu stellen. Wenn Du Dich für das Menschliche innerhalb der rechtlichen Fragen interessierst, leidenschaftlich bist etwas beizutragen und Einblicke in eine mögliche Karriere in einem in-house Legal Team in der Privatwirtschaft bekommen möchtest, könnte dies die ideale Rolle für Dich sein. Wir bieten ein 6-monatiges juristisches Volontariat vom 1. Juni 2025 bis zum 30. November 2025 an. Deine Aufgaben umfassen: Du unterstützt unser Rechtsteam bei der Beratung im Bereich des Arbeitsrechts, einschliesslich Fragen zu Diversity, Equity & Inclusion, sowie bei Gerichtsverfahren und internen Untersuchungen. Dabei hast Du die Möglichkeit, komplexe globale und lokale Rechtsfragen anzugehen und Herausforderungen in Lösungen zu verwandeln. Du übernimmst praktische Aufgaben, indem Du sowohl individuelle Rechtsfälle als auch grosse Projekte wie Reorganisationen, Veräusserungen und die Implementierung neuer Richtlinien und Prozesse betreust. Zudem entwirfst und überprüfst Du Verträge, interne Regelwerke sowie Vorlagen. Dies ist Deine Chance, von der Theorie zur praktischen Anwendung zu wechseln und direkt etwas zu bewegen. Deine Aufgaben umfassen zudem tiefgehende juristische Abklärungen und die Erstellung von Rechtsmemoranden, die uns helfen, komplexe Rechtsfragen in verständliche Erkenntnisse umzuwandeln. Darüber hinaus spielst Du eine entscheidende Rolle bei der Berichterstattung über wichtige rechtliche Angelegenheiten an unsere Prüfungsausschüsse in strikter Übereinstimmung mit dem Sarbanes-Oxley Act. Was Du für die Rolle mitbringst: Schweizer Bachelor of Law (BLaw) und Master of Law (MLaw) Sehr gute Sprachkenntnisse in Englisch und Deutsch, sowohl mündlich als auch schriftlich Hohe Motivation und die Fähigkeit, unabhängig an herausfordernden Aufgaben und Projekten zu arbeiten Frühere juristische Praktika und Kenntnisse im Arbeitsrecht sind von Vorteil Bist Du bereit, Deine Fähigkeiten zu verfeinern und aktiv Veränderungen mitzugestalten? Wenn Du begeistert davon bist, Neues zu lernen und unser Team in der täglichen Arbeit zu unterstützen, dann bewirb Dich jetzt und reiche ein Motivationsschreiben ein, das Deine Beweggründe für die Bewerbung auf diese Stelle darlegt und Deine Verfügbarkeit für den 1. Juni 2025 bestätigt. Wir freuen uns auf Deine Bewerbung! Warum Novartis? Unser Vorsatz ist es, die Medizin neu zu gestalten, um Menschenleben zu verbessern und zu verlängern. Unsere Vision ist es, das wertvollste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie wir das erreichen werden? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns tagtäglich dazu antreiben, unsere Ziele zu erreichen. Werden Sie Teil dieser Mission und dieses großartigen Teams! Erfahren Sie hier mehr: https://www.novartis.com/about/strategy/people-and-culture Was wir bieten: Alle Informationen finden Sie in unserem Novartis Life Handbook (Englisch): https://www.novartis.com/careers/benefits-rewards Barrierefreiheit und Unterstützung: Wenn Sie aufgrund einer Erkrankung oder Behinderung spezielle Unterstützung während des Rekrutierungsprozesses brauchen und/oder deswegen detailliertere Informationen über die wesentlichen Funktionen einer Stelle benötigen, senden Sie bitte eine E-Mail an diversity.inclusion_ch@novartis.com und teilen Sie uns die Art Ihres Anliegens und Ihre Kontaktinformationen mit. Bitte vergessen Sie nicht, dabei die Referenznummer der Stellenausschreibung anzugeben. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Position nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber dennoch mit uns in Kontakt bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann treten Sie hier dem Novartis Netzwerk bei: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Legal Business Unit Corporate Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Job Type Full time Employment Type Praktikant*in/Student*in (Befristet) Shift Work No

Job ID REQ-10023256 Oct 11, 2024 Switzerland Summary We are looking for a GCP Bioanalysis Senior Scientist in the Translational Medicine Drug Disposition Bioanalytical group. The role involves using bioanalytical knowledge and lab/instrument skills to develop, validate, and analyze clinical samples for the company's novel modality biologics portfolio. Responsibilities include independently designing and validating assays, performing sample analysis, processing data, and evaluating results. As Senior Scientist you will also contribute to health authority documents, maintain lab equipment and records, and mentor team members. The ideal candidate has a college/university degree in biological sciences, experience in regulated biologics bioanalysis, proficiency in various biological techniques, and the ability to work independently and meet deadlines. About the Role In the Senior Scientist role, you will use your knowledge of bioanalytics and lab/instrument skills to develop, validate and analyze clinical samples focusing on our novel modality biologics portfolio. Key responsibilities: Independently designing, developing, and validating assays, and performing sample analysis using biological techniques for PK, PD and immunogenicity following SOPs and guidelines. Being responsible for all assigned study/lab/project activities, and providing input to bioanalytical strategies. Data processing, evaluating results, interpreting data, and drawing relevant conclusions. Critically analyzing data on study and project levels. Conducting lab activities and keeping timely raw data records in accordance with company and health authority guidelines. Preparing study protocols, reports, and contributing to health authority documents. Maintaining high level of competence on routinely used laboratory equipment and/or LIMS systems. Evaluating and setting up new technologies as they are introduced to the lab. Contributing to the general lab environment, including instrument maintenance, writing/updating templates and SOPs, software validation activities, ordering supplies, etc. Coaching and mentoring in a matrix team environment. Essential requirements: College/university degree in biological related sciences or equivalent, with 3+ (Masters) or 5+ (Bachelors) years of experience. Experience in regulated biologics bioanalysis preferred. Strong laboratory skills with proficiency in several biological techniques (ELISA, ECL, PCR, etc.) and their associated software. Ability to work with minimal supervision and organize work across multiple projects to meet timelines Eagerness to take on additional responsibilities when required; flexibility to adapt to changing priorities and strategies. A collaborative spirit and willingness to mentor/coach peers Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You-ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams- representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10022054 Oct 11, 2024 Switzerland Summary The Operational Planner (OP) ensures adherence to the production plan including timely availability of all materials in accordance with GMP rules. The OP coordinates the availability of resources and the implementation of the production plan with the shop floor in GCS. Execute and monitor timely activities related to assigned area of responsibility under the guidance and accountability of more senior associates. About the Role The Operational Planner (OP) ensures adherence to the production plan including timely availability of all materials in accordance with GMP rules. The OP coordinates the availability of resources and the implementation of the production plan with the shop floor in GCS. Execute and monitor timely activities related to assigned area of responsibility under the guidance and accountability of more senior associates. Key responsibilities: Executes production plan on time in full on a short-term operational horizon. Releases shop orders in SAP for internal packaging and allocates pack materials. Creates the print orders in SAP and orders the overprinted labels to the 3rd party label vendors where required. Manages the invoices (check and approval) from the 3rd party label vendors. Manages production supply area by ensuring components of BOMs are available (staging) and by monitoring expiry date and status. Leads weekly meeting with shop floor to ensure feasibility of production plan Collaborates with role responsible for Production Master Data regarding BOMs and recipes. Identifies and mitigates risks on short term planning updates, with appropriate escalation and communication. Implements actions to resolve backlogs in coordination with the shop floor (shift, resource, short term personnel planning change, overtime) Collaborates with the Tactical Planner for handover processes. Proactively communicate key issues and any critical topic in a timely manner to the appropriate management level and to/or any other relevant project team members. Provide input on issues and collaborates with other team members to facilitate issues resolution. Key performance indicators: Quality (GMP), quantity, and timelines for all assigned tasks/projects -Compliance with Novartis standards, in particular, ethics, health, safety, and environment (HSE), and information security (ISEC) standards. Unit KPIs (e.g. FPFV (first patient first visit), LTA (lost time accident), FTR (first time right), Rework Rates, Recalls) Essential requirements: Degree in science, engineering or equivalent. 2 years of practical experience in chemical / pharmaceutical industry or 3 years of experience in field of expertise Apprenticeship or formal education in a logistical, technical or related business area Basic project management, good organization and planning skills Good knowledge of HSE/GMP standards and processes Problem-solving and idea generation skills Good presentation skills Fundamental Leadership skills. Good communication, negotiation and interpersonal skills. Ability to work in interdisciplinary teams. Proficient in English. Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You-ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams- representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No

Du liebst es, tagtäglich an der frischen Luft mit deinen Kompetenzen als Strassenbauer deine Kundschaft zu überzeugen? Intakte Strassen, Wege und Werkleitungen sind dir wichtig? Für unseren Kunden, ein kleineres Strassen- und Tiefbauunternehmen im Raum Basel, suchen wir dich als ihren neuen Strassenbauer.zurück zur SucheStrassenbauer im Raum BaselStellenbeschriebAnforderungsprofil Grundausbildung als Strassenbauer (Verkehrswegbauer) oder Tiefbauer Mindestens 3 Jahre Berufserfahrung Werkleitungsbau (Gas, Wasser; Strom) Erd-, Beton-, Belagsbau Erstellen von Entwässerungseinrichtungen Fundationsschichten Randabschlüsse und Einbau bitumenhaltiger Beläge Umgang mit Minibagger, Radlader und Dumper von Vorteil Gute Plankenntnisse Selbstständiges Arbeiten (evtl. Führen von Hilfskräften) Belastbarkeit und Flexibilität Freude an Teamarbeit PW-Ausweis von grossem VorteilAngebot Flache Führungsstrukturen Langjährig eingespieltes Team Interessante Bauobjekte in der Innenstadt von Basel Marktgerechter Lohn Gute Sozialleistungen Selbständiges Arbeiten Hoher VerantwortungsgradBist Du an der offenen Stelle als Strassenbauer interessiert? Dann fülle das nachstehende Kontaktformular aus und lade deine vollständigen Bewerbungsunterlagen hoch. Wir melden uns in den nächsten Tagen bei dir.Online seit dem:08.01.2024Stellenart:Temporär und FestArbeitsort:BasellandAusbildung:Strassenbauer EFZ / Verkehrswegebauer EFZ oder mehrjährige BerufserfahrungKontaktformularWeitere Ergebnisse der BrancheAsbestsanierer im Raum BaselOnline seit:07.01.2024Standort:Basel & BasellandAusbildung:Grundkenntnisse in der Asbestsanierung, allgemeine SchadstoffsanierungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben ührer im Raum Basel (Kleinbagger bis 9t)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Einige Jahre Erfahrung als BaumaschinistKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum Basel (Hochbau)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Mehrjährige Berufserfahrung als BauarbeiterKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum Basel (Umbau)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Mehrjährige Erfahrung als Bauarbeiter im UmbauKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:09.01.2024Standort:LiestalAusbildung:Baumaschinist mit entsprechender ErfahrungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum Basel (Strassenbau)Online seit:09.01.2024Standort:Basel-StadtAusbildung:Mehrjährige Erfahrung als Bauarbeiter im StrassenbauKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:07.01.2024Standort:BasellandAusbildung:Ausbildung zum Baumaschinenmechaniker oder langjährige BerufserfahrungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben / Kernbohrer im Raum BaselOnline seit:08.01.2024Standort:Basel-StadtAusbildung:Ausbildung zum Betontrenner oder mehrjährige ErfahrungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:08.01.2024Standort:Basel-StadtAusbildung:Baupolier mit eidg. Fachausweis oder langjährige BerufserfahrungKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:08.01.2024Standort:BasellandAusbildung:Grundausbildung Betontrennfachmann oder mehrjährige ErfahrungKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben ührer im Raum BaselOnline seit:07.01.2024Standort:Basel-StadtAusbildung:Kranführerausweis BKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben ührer im Raum Basel (Kabine)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Kranführerausweis BKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum Basel (Kundenbereich)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Ausbildung zum Maurer oder mehrjährige Berufserfahrung als KundenmaurerKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben im Raum Basel (Kundensegment)Online seit:08.01.2024Standort:Basel-StadtAusbildung:Grundausbildung als Maurer EFZ, Weiterbildung als Vorarbeiter oder mehrjährige BerufserfahrungKontakt:Ivan Morales+41 61 560 19 E-Mail schreiben ästerer im Raum BaselOnline seit:07.01.2024Standort:Basel-StadtAusbildung:Mehrjährige Erfahrung als PflästererKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:09.01.2024Standort:Basel-StadtAusbildung:Grundkenntnisse in der SchadstoffsanierungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben Hochbau im Raum BaselOnline seit:09.01.2024Standort:Basel-StadtAusbildung:mehrjährige Erfahrung als SchalerKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:07.01.2024Standort:Basel-StadtAusbildung:Ausbildung zum Bau-Vorarbeiter oder langjährige BerufserfahrungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben im Raum BaselOnline seit:09.01.2024Standort:BasellandAusbildung:Ausbildung zum Strassenbau-Polier mit eidg. Fachausweis oder mehrjährige BerufserfahrungKontakt:Santiago Insua+41 61 560 19 E-Mail schreiben

Arbeite mit unsOffene StellenDie Sauter Wärmetechnik GmbH, der Spezialist rund ums Heizen sucht:Heizungsinstallateur EFZ (m/w)per sofort oder nach VereinbarungAusführung von Tankrevisionen, Tankstillegungen und Sichtkontrollen. Mithilfe bei Heizungsinstallationen als Allrounder.Wir erwarten: Installationen von allen Heizsystemen im Neu- und Umbau wie z.B. Öl-, Gas-, Wärmepumpen und Solar Rohrinstallationen Kleinere Schweissarbeiten autogen Handwerkliches Geschick und technisches Verständnis Sauberes, selbständiges und verantwortungsvolles Arbeiten Freundlicher und korrekter Umgang mit Mitarbeitern und KundenWir bieten: Mitarbeit in einem motivierten und aufgestellten Team Zeitgemässe Anstellungsbedingungen (Mitglied Suissetec) Weiterbildungsmöglichkeiten Vielfältige Auftragsgebiete von Grossbaustelle bis EinzelkundeHaben wir Ihr Interesse geweckt? Zögern Sie nicht und senden uns per E-Mail Ihre vollständigen Bewerbungsunterlagen inklusive Foto. Für vorgängige Fragen stehen wir Ihnen gerne zur Verfügung

Mission temporaireNous recherchons pour un de nos clients renommé sur la place Genevoise, dans le domaine de la physiothérapie à domicile.un(e) physiothérapeute à 60%Bénéficiant dexcellentes conditions de travail, une grande autonomieVous intégrerez une équipe jeune et dynamique, il sun poste varié.Envoyez nous votre dossier complet, nous reviendrons rapidement vers vous si celui correspond à nos E-Mail schreiben .pdf privilégié inférieur à 5 Mo

<div class="jobs-item jobs-single-item"><div class="position-header"><h1>Bau- und Projektleiter/in</h1><h2 style="padding-top:5px;"><span>8005 Zürich</span></h2></div><p><span>Wo ein Wille ist, ist auch ein Weg! Nach diesem Leitsatz führt unser Kunde aus dem Raum Zürich sein Unternehmen. Unser Kunde, verantwortlich für die Realisierung von anspruchsvollen Projekten im Um- und Neubau-Bereich, suchen wir zur Verstärkung des motivierten Teams </span><strong>eine/n motivierte/n Bau- und Projektleiter/in.</strong><span> Eintritt ist per sofort oder nach Vereinbarung.</span></p><br/><p><strong>AUFGABEN</strong></p><ul><li>Sie planen, organisieren und überwachen die diversen Bauabläufe</li><li>Sie verhandeln mit Unternehmern und bringen hierzu das nötige unternehmerische Denken und Handeln mit</li><li>Sie führen und überwachen die Unternehmer auf den Baustellen</li><li>Sie optimieren die Bauabläufe und übernehmen die Verantwortung für Qualität, Termine und Kosten</li></ul><br/><p><strong>ANFORDERUNGEN</strong></p><ul><li>Sie haben mehrere Jahre praktische Erfahrung in der Bauleitung in der Schweiz</li><li>Sie haben gute Erfahrungen in den gängigen Bauadministration und Terminplanungsprogrammen (Messerli, MS-Projekt)</li><li>Sie Bringen selbständige Arbeitsweise, Belastbarkeit, lösungsorientiertes Denken mit</li><li>Sie besitzen sehr gute Deutschkenntnisse</li></ul><br/><p>Sind Sie eine unser Mann? Wollen Sie im Leben endlich einen Schritt weiterkommen, in jeder Beziehung? Arbeiten Sie gerne selbständig und wollen Sie sich auf unsere Kosten laufend weiterbilden? Dann wollen wir Sie unbedingt kennenlernen.</p><p>Fragen zur Stelle? Herr Aydin Altas gibt Ihnen gerne unter 044 200 79 73 oder E-Mail schreiben weitere Auskünfte.</p><p>Bitte legen Sie Ihrer Bewerbung einen Lebenslauf und Unterlagen Ihrer fachlichen Qualifikationen bei und senden Sie diese an uns zu.</p><p>Hinweis: Bitte beachten Sie, dass Bewerbungen per Post gerne bearbeitet, jedoch aus administrativen Gründen nicht retourniert werden. Wir freuen uns auf Ihre Bewerbung.</p><div class="clearfix" style="margin-top:20px;"><a class="btn btn-secondary" href="/Vacancyboard/Apply/28823">Bewerben</a><ul class="social-links pull-right" style="font-size:15px;vertical-align: middle !important;padding-top:5px;padding-bottom: 5px;"><li><a href="#"><i class="fa fa-facebook"></i></a></li><li><a href="#"><i class="fa fa-twitter"></i></a></li><li><a href="#"><i class="fa fa-google-plus"></i></a></li></ul><span class="pull-right" style="padding-right:10px; padding-top:10px; padding-bottom: 10px;font-size:13px;vertical-align: middle !important;"><strong>Teilen</strong></span></div></div>

Job ID REQ-10023921 Sep 27, 2024 Switzerland Summary Location: Basel, Switzerland, or Cambridge, MASS, US Lab Solutions & Scientific Services, situated within the Scientific Operations (SO) organization, is responsible for providing integrated programs and services that support our scientific community, and has a mission to enable the Novartis BioMedical Research-s (BR) lab scientists to focus on science in the lab through data-driven, sustainable operational excellence and innovation. Lab Solutions & Scientific Services consists of four global sub-functions and this role provides global leadership working in the key area of lab equipment management. We are now seeking an experienced Lab asset management expert, ideally with a strong Biology background to join us as a key member of the global Lab Equipment Management (LEM) program team. About the Role You will ensure the success of the end-to-end lab equipment management program by building strong partnerships with the local operations community, the Asset Strategy Governance Board (ASGB), equipment category SMEs, and other Biomedical Research stakeholders and support functions. Specifically, you will manage the Biomedical Research LEM program end-to-end within your category, including interactions with engaged third parties and support from the local Lab Equipment Operations team. Responsibilities include: Coordinate and chair the global Asset Strategy Governance Board (ASGB) within your category. Develop a global equipment life cycle strategy within your category, collaborating with ASGB, SMEs, Disease Area/Finance Area operations, data analyst, lab equipment operations, procurement, and vendors. Regularly update and maintain the plan based on shifting priorities and changes. Document and maintain life cycle plans, ASGB decisions and guidance documents on Biomedical Research standards within your category, using standard templates within the LEM program. Report key LEM program performance indicators regularly Review and align equipment demand requests with the global strategy within your category, identifying opportunities for bundling and aligning priorities with finance across categories. Align with internal stakeholders on vendor negotiations for CapEx, global service contracts, and consumables with key vendors within your category. Prepare for Capital Acquisition Request (CAR) review at the Investment Review Meeting (IRM) for equipment with an overall strategy and life cycle plan and communicate approvals back to DAs/FAs. Coordinate bundled sourcing across Biomedical Research with involved DAs/FAs. Collaborate closely with finance to manage the budget for the equipment category based on global strategies and forecasting. Minimum Requirements - What you will bring to the role Bachelors, Masters or equivalent in relevant scientific (ideally Biology) discipline with appropriate years of industry experience in a relevant field within drug discovery or related area. Proven experience in enterprise strategic planning and asset management. Strong technical skills and experience in the equipment category Excellent vendor relations management and negotiation skills Strong leadership skills and the ability to work cross-functionally with various teams and stakeholders. Ability to influence without authority and actively manage key stakeholders Project Management experience and Lean and Six Sigma experience a plus Ability to exercise independent discretion and judgment to solve problems as well as an ability to prioritize effectively in a fast-paced and dynamic environment. Strong understanding of the processes and protocols required in a scientific research organization. Proficiency in using IT tools to capture, manage and analyze data required (e.g. MS Excel, SharePoint & Access, Spotfire, SAP) Excellent communication skills with ability to present information to operations leadership and scientific customers (fluent English with German language considered an advantage) Demonstrated problem-solving and analytical skills and recommend process changes when appropriate Solution-oriented individual with a proven track record of problem solving Broad knowledge of discipline, methods and technologies *Restrictions on flexible working arrangements may apply and will be discussed at interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<div class="card col-12"><br/><div class="card-body"><div class="row"><div class="col-3"><img alt="Chef de Partie (m/w) 100% " class="card-img-top" src=" https://www.offene-stellen.ch/topcmsimages/Auf5ff5a9b32c5cc_Auf5b86b77a73c86_swisslinkpersonals.jpg"/&gt;&lt;br/&gt;&lt;/div&gt;&lt;div class="col-9"><h1 class="card-title title">Bauarbeiter / Hilfsarbeiter (Tiefbau) - Stellenbeschreibung 543862</h1><h2>Stelleninserat von <a href="Stelleninserate-1317.php" title="Stellenangebote von SWISS LINK">SWISS LINK</a></h2><p><i class="fa fa-calendar"></i> 16.10.2024 / <i class="fa fa-globe"></i><strong>Arbeitsort:</strong> Riedikon ZH <br/>Telefon: <a href="tel:41(0)552206040" rel="nofollow">41 (0) 55 220 60 40</a><br/>Jobs in Riedikon ZH </p></div></div><p class="card-text"><h2>Zur Stelle:</h2> Mittelgrosse Hoch- und Tiefbauunternehmung / allg. Hilfsarbeiten im Tiefbau (Baugruben, Schächte, Gräben für Strassen, Böschungen, Randbefestigungen, verlegen von Rohren, etc.) / Baustellen praktisch nur im Zürcher Oberland / Aushilfe im Erdwärmesondenbereich oder auf dem Hochbau erwünscht / zuerst Temporär (Probezeit)- und nach 3 Monaten Festanstellung </p><p><div class="d-grid gap-2"><a class="btn btn-primary btn-block" href="kontakt.php?ID=543862" rel="nofollow" title="Stellenbewerbung">Jetzt bewerben</a></div></p><h3><span>Anforderungen</span></h3><p><p>Baustellenerfahrung auf dem Bau zwingend (von Vorteil auf dem Tief- oder Strassenbau) / bis max. 45 Jahre jung / mind. Baustellendeutsch verstehen / mobil oder in der Nähe von Riedikon (bei Uster ZH) wohnhaft / gerne auch Bewerber aus dem Ausland (ein Zimmer und die Arbeitsbewilligung kann für EU - Bürger organisiert werden) </p><h3>Anstellungsart</h3><p>Fest</p><h3>Antrittsdatum</h3><p>Nach Vereinbarung </p><h3>Ausbildung / Erfahrung</h3><p>Unbestimmt</p><h3>Kontakt / Ansprechpartner</h3><p>SWISS LINK<br/>Swiss Link<br/>8640 Rapperswil-Jona</p><p>Ihr Personalberater Otti Feldmann <br/><a href="tel:41 (0) 55 220 60 40" rel="nofollow">41 (0) 55 220 60 40</a><br/><a href=" E-Mail schreiben " rel="nofollow">Mail</a></p><br><a href=" https://www.swisslinkpersonal.ch " rel="nofollow" target="_blank">Website</a><br/><h4>Region(en)</h4><p><img alt="Riedikon ZH" class="img-fluid img-thumbnail lazyload" data-src=" https://www.offene-stellen.ch/Bilder/4Kt.gif " title="Jobs Bauarbeiter / Hilfsarbeiter (Tiefbau)"/><p>Schweiz / Kanton St. Gallen</p><iframe allowfullscreen="" height="400" src=" https://maps.google.de/maps?hl=de&amp;q=Riedikon+ZH&amp;ie=UTF8&amp;t=&amp;z=10&amp;iwloc=B&amp;output=embed " title="Arbeitsort" width="100%"></iframe>

<p><p>Die Spitex Zürichsee leistet mit ihrem Angebot an Pflege und Betreuung einen wichtigen Beitrag zur Gesundheitsversorgung und zur Erhaltung hoher Lebensqualität im gewohnten sozialen Umfeld. Sie bietet für alle Einwohnerinnen und Einwohner der Gemeinden Erlenbach, Herrliberg, Männedorf, Meilen und Uetikon am See Leistungen im pflegerischen und hauswirtschaftlichen Bereich an. Dabei arbeitet sie mit Ärzten, Heimen und Spitälern sowie anderen im Gesundheitsbereich tätigen Organisationen zusammen. Sie verfügt als Non-Profit- Organisation über einen Leistungsauftrag der vorerwähnten Trägergemeinden und beschäftigt rund 130 Mitarbeitende.</p><p>Zur Verstärkung unseres Teams suchen wir per sofort oder nach Vereinbarung eine/en</p></p><p>Assistent/in Gesundheit und Soziales (AGS)</p><p><p><strong>Deine Aufgaben</strong></p><ul><li>Grund- und Behandlungspflege bei den Klientinnen und Klienten</li><li>Selbstständige Durchführung von hauswirtschaftlichen Einsätzen gemäss Vereinbarung </li><li>Beobachtung der Situation bei den Klientinnen und Klienten und Meldung, bei Veränderungen sowie potentiellen Gefahren, an die verantwortliche Stelle</li><li>Sicherstellung der Qualität, Hygiene und Arbeitssicherheit gemäss betrieblichen Richtlinien im Verantwortungsbereich</li></ul><p><strong>Das bringst du mit</strong></p><ul><li>Abgeschlossene Ausbildung als Assistent/in Soziales und Gesundheit EBA</li><li>Berufserfahrung in der Langzeitpflege oder Spitex von Vorteil</li><li>Selbstständige Arbeitsweise sowie verantwortungsvolles und engagiertes Handeln</li><li>Hilfsbereitschaft und Verständnis für individuelle Bedürfnisse sowie Geduld und Respekt</li><li>Gute Kommunikationsfähigkeiten, Belastbarkeit und Teamfähigkeit</li><li>EDV-Anwenderkenntnisse von Vorteil, insbesondere Erfahrung mit Perigon</li><li>Gute Deutschkenntnisse in Wort und Schrift (mindestens Niveau B2)</li><li>Führerausweis Kat. B und ein eigenes Auto von Vorteil</li></ul><p><strong>Wir bieten dir</strong></p><ul><li>eine vielseitige, verantwortungsvolle Aufgabe in einem spannenden Umfeld am schönen Zürichsee</li><li>Eine abwechslungsreiche Tätigkeit</li><li>moderne Arbeitsinstrumente (eigenes Tablet)</li><li>attraktive Anstellungsbedingungen</li><li>Unterstützung bei Deiner fachlichen Weiterbildung</li></ul><p> </p><p>Wenn Du Dich angesprochen fühlst, freuen wir uns auf Deine vollständigen Bewerbungsunterlagen per E-Mail an <a href=" E-Mail schreiben " target="_blank"> E-Mail schreiben </a>.</p><p>Wir freuen uns darauf, Dich kennenzulernen!</p></p>

Job ID REQ-10020610 Sep 09, 2024 Switzerland Summary Responsible for delivery and oversight of submission readiness of clinical documents, to support authoring formatting, and publishing of clinical documents required for regulatory submissions, and achieve rapid, accurate and timely submissions to health authorities. Drives implementation of CDGM initiatives, projects and process improvement activities to enhance clinical document management systems, processes and standards at Novartis. About the Role Major Accountabilities (Describe the 5-7 main results of the role to be achieved) Responsible for efficient and appropriate management of submission-relevant documentation (e.g., Protocol, CSR, ICF, PDR, etc.) for global clinical,) to meet electronic publishing requirements, Health Authority guidelines, Good Clinical Practices and Novartis SOPs. Coordinate and oversee the authoring and finalization of the CSR appendices for assigned studies. Support implementation of the submission document readiness management strategy for clinical documents and clinical documents templates. Executes vendor oversight plan, monitors service metrics and identifies opportunities for improvement to the operating model. Acts as point of escalation for issues. Develop and maintain submission readiness processes, contribute to or drive initiatives to improve and innovate business and technical aspects of submission readiness activities, in collaboration with other CDGM groups, business and IT Functions. Collaborate with cross-functional stakeholders (e.g., Regulatory Writing & Submissions, Regulatory Affairs, Trial Management, etc.) on the planning, preparation, and delivery of high-quality documents within timelines, including expedited support for urgent requests to meet regulatory deadlines. Identify and communicate processing risks/trends/patterns related to regulatory submission documents and works with key stakeholders to define and implement appropriate remediations. Serves as Subject Matter Expert on Regulatory Document Manager training materials, formal and informal processes, and tracking tools for submission readiness oversight activities in collaboration with CDM Process team and other key stakeholders. Provides Audit/Inspection support, contributes to root cause analysis identification and creation/delivery of CAPAs. Minimum Requirements: Bachelor-s degree in life-sciences/healthcare/pharmacy/information management and relevant industry experience. Languages: English fluency (written, oral) required. Relevant Experiences : Thorough knowledge of clinical document management processes Advanced knowledge of clinical documentation practice guidelines & principles (Good Documentation Practice, Data integrity, ICH eCTD and FDA Portable Document formatting specifications (PDF) guidance) Experience of authoring, compilation and formatting of CSR appendices according to ICH E3 3-5 years in clinical development/clinical operations or similar business area 2-3 years working experience with document management systems and excellent understanding of system structures and generic document management functionality Good understanding of technical processes and PC environment including Microsoft suite of products Advanced ability to work independently Experience with project work or project management in a global, cross- functional multicultural and international matrix organization Excellent communication, organization and tracking skills Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10025321 Oct 09, 2024 Switzerland Summary Join the Novartis Patient-Centered Outcomes (PCO) Center of Excellence in Development for a Postdoc assignment in a cross-functional and cross-divisional environment. Advance your knowledge on PCOs, Digital Endpoints, and Patient Experience and Preference insights and data while building a network across Global Program Teams, Patient Engagement, Digital Endpoints Capability Center, and Value & Access Patient Centered Outcome Strategy. About the Role Join the Novartis Patient-Centered Outcomes (PCO) Center of Excellence in Development for a Postdoc assignment in a cross-functional and cross-divisional environment. Advance your knowledge on PCOs, Digital Endpoints, and Patient Experience and Preference insights and data while building a network across Global Program Teams, Patient Engagement, Digital Endpoints Capability Center, and Value & Access Patient Centered Outcome Strategy. Duration: 1 year Preferred start date: January 2025 Your responsibilities will include: Assess the Clinical Outcome Assessment (COA) status in new indications and determine the suitability of existing COA measures and Digital Health Technologies Partner with different functions of Development and Value & Access to develop COA and Digital Endpoint strategies for individual programs Advance the patient-centric culture in Novartis. Support the implementation of a patient engagement and patient experience data framework and related change management initiatives, training and communication, Develop and contribute to the conduct of training sessions to advance the knowledge of 5,000 Novartis associates regarding Patient-Reported Outcomes and Patient Experience Data Develop and publish posters and manuscripts What you-ll bring to the role: Recent Postdoc with medical or scientific degree (MD or PhD) Knowledge of Patient-Reported Outcomes and interest in patient-centered drug development Clinical research experience Proven ability to work in cross-functional teams Project Management Skills Structured approach, attention to detail, taking task ownership through to successful delivery Business-level written and spoken English. Advanced IT literacy, quickly learning new technology Please submit your CV and a cover letter describing your motivation and qualification for this role and from when you will be available. Thank you. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com, and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Others Job Type Full time Employment Type Early Talent (Fixed Term) Shift Work No

Job ID REQ-10022153 Oct 09, 2024 Switzerland Summary Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people-s lives. To do this, we are optimizing and strengthening our processes and ways of working as well as innovating the way we design our clinical trials. We are investing in new technologies and building specific therapeutic areas and platform depth and capabilities - all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to. Apply today and we can thrive together! About the Role Are you ready to become the Associate Director, Clinical Development Advanced Methods? This is a pivotal role within Clinical Development, whereby the individual will be instrumental in applying advanced methods and innovative designs to accelerate drug development programs, increase trial success and advanced label claims. This role interlinks with key business functions such as Analytics, Regulatory Affairs, Medical Affairs and Early Development. So, if you have an eye for identifying and evaluating cross functionally applicability and implementability of organisationally aligned advanced methods in clinical development then you should apply. Major accountabilities but not limited to: Partner and deputize the Global Head of Advanced Methods as the Clinical Development representative for enterprise-wide innovation projects. Support development and maintenance of a strategic concepts, in partnership with the Global Head Advanced Methods, to drive advanced trial designs and methodologies to clinical development plans and study designs within the Development organization. Support clinical teams with implementation of these concepts applying a nimble and agile approach leveraging existing expertise. Identify, drive and support innovative projects relevant to clinical trial design and clinical development plans Proactively monitor internal and external trends in clinical development to identify new trials designs and methods. Key performance indicators: Quality & consistency of evaluating and creating organizational alignment on prioritized focus areas for advanced methodologies. Quality & consistency in raising awareness and disseminating Advanced Methods opportunities across the organization. Quality & consistency of cross-functional support provided to program team driving internal uptake and external acceptance. Influencing external environment aligned with our strategic goals e.g. regulators, trade association, KoL, scientific societies, academics. Identification of internal and external trends (competitive intelligence and horizon scanning) Your Experience: Advanced life science degree (Ph.D, PharmD, Master in Public Health). Minimum 10 years of relevant experience in pharmaceutical industry preferably across several disease areas and development phases Working knowledge of Drug Development processes, with extensive experience in designing and conducting clinical trials, with a deep understanding of regulatory requirements and guidelines. Successful relationship builder and communicator with experience leading cross-functional work streams, driving program excellence and engaging functional partners Fluent in English Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity & Inclusion : Novartis is committed to building an outstanding, inclusive work environment and diverse team-s representative of the patients and communities we serve. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10019694 Sep 05, 2024 Switzerland Summary Multiple Positions Available. This position will be located in Cambridge, MA USA or Basel, Switzerland but can not be located remotely. #LI-Hybrid About the role: We are building a novel non-clinical statistics function within our Data Science and Modeling and Simulation team in PK Sciences which is part of our Translational Medicine Organization. We are seeking an Associate Director Non-Clinical Statistics, who can independently support one of our key disease areas. This role engages with scientists, project teams, and disease areas across Biomedical Research. About the Role Major accountabilities: · Collaboration: Work closely with scientists, project teams, and disease areas to integrate statistical methodologies into research and development processes. · Statistical Support: Provide expert statistical support for non-clinical studies, ensuring robust data analysis and interpretation. · Innovation: Contribute to the development and application of innovative statistical techniques · Training and Mentorship: Mentor junior statisticians and data scientists, promoting a culture of continuous learning and professional growth.. · Cross-Functional Representation: Represent non-clinical statistics on cross-functional teams to provide effective statistical consideration and collaborate closely with scientists across Biomedical Research. · Statistical Approaches: Ensure and implement statistically sound approaches for the design, analysis, reporting, and interpretation of exploratory and regulatory non-clinical studies. Automation Development: Develop automated solutions Education: Ph.D. or Masters in Statistics, Biostatistics, or a related field strongly preferred. Experience: Minimum of 6 years of experience in non-clinical statistics, with a strong working knowledge in biology, pharmacology and toxicology. Technical Skills : Expertise in statistical software and programming languages (e.g., R, SAS, Python). Communication: Excellent communication and interpersonal skills, with the ability to engage effectively with diverse stakeholders. Innovation: Demonstrated ability to drive methodological innovation and apply advanced statistical techniques to complex problems. Fluent in English (oral and written). Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10019278 Sep 05, 2024 Switzerland Summary Location: Basel, Switzerland Full time, onsite, #LI-onsite Novartis' Biomedical Research division is our Innovation engine. Within our ground-breaking Radioligand Therapy Labs in our Oncology division we have ambitions to transform the lives of millions of people living with cancer and focus in powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Applications are invited for a scientific associate to carry out cutting-edge oncology drug discovery and pharmacology research. We seek an experienced, motivated and ambitious individual with a passion for in vivo oncology research. You will join the Radioligand Therapy team to develop and validate novel targets in our world leading Oncology portfolio. About the Role The ideal candidate should have a passion for working with rodents and a drive to perform in vivo oncology pharmacology studies including micro-surgeries, compound administration and preparation of samples for ex vivo analysis. Hands-on background performing small animal imaging modalities such as PET/SPECT/uCT or in cell biology techniques is a plus. The successful candidate will work collaboratively as an integral part of global projects and be an active member of lab and project teams. Responsibilities include but are not limited to: Develop and characterize novel in vivo oncology models Perform efficacy studies with cutting edge radioligand therapies Perform biodistribution studies and metabolites analysis Perform pre-clinical imaging studies including PET/SPECT/uCT Design, perform and evaluate various in vitro and ex vivo assays (e.g. cell culture, transfections, IHC, proliferation assays, immunofluorescence, PCR, Western blotting, FACS) Minimum requirements What you-ll bring to the role: Masters degree in pharmacology, cell biology, medical physics, bioengineering, biotechnology or related field or Bachelors degree with equivalent experience Practical work experience in biomedical research from an industry or academic laboratory Experience in performing animal studies (animal handling, drug application, sampling, animal welfare regulations, small laboratory animal surgery) Self-motivated, proactive, and able to work independently Desired: Knowledge and experience of standard cell biology techniques is desirable: cell culture, IHC, FACS, quantitative real-time PCR, transfection, western blotting, cell engineering etc Highly collaborative team player that enjoys working across multi-disciplinary teams Excellent organizational and communication skills Knowledge of cancer biology * This position is eligible for 80-100%* working time, however, some restrictions on flexible working options may apply and will be discussed during interview if applicable. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10018599 Sep 05, 2024 Switzerland Summary Location: Basel, Switzerland Full time, onsite, #LI-onsite Within our Oncology and Radioligand Therapy labs we have bold objectives to transform the lives of millions of people affected by cancer. The Oncology Translational Research (OTR) Department at Novartis Biomedical Research is a global, laboratory-based research group, supporting the development of novel therapeutics in the Novartis Biomedical Research Oncology Disease Area. About the Role Within OTR, the Oncology Pathology and Biomarkers (OPB) group uses tissue-based, cell-based and soluble protein assays to understand target epidemiology and biology, mechanisms of action of drugs, and response/resistance biomarkers, ranging from early stages of target identification through Phase 3 clinical trials. OPB is seeking a motivated and curious PhD qualified scientist to design and conduct imaging-based experiments for developing clinical biomarker strategies that advance Novartis Oncology drug candidates. The candidate will partner across the full range of Oncology programs (radioligand therapeutics (RLT), small molecules and biotherapeutics) with a special focus on the effects of RLT on preclinical models and human tissues. This role will involve correlating immunohistochemistry and other imaging techniques with radioligand imaging results to answer key questions related to these therapies. The ideal candidate is passionate about tissue-based biomarker assay development (e.g., IHC, ISH, and FIHC), has a background in imaging, and possesses a keen interest in innovative experimental design. Key responsibilities: Design and conduct experiments and procedures requiring scientific and technical knowledge of immunohistochemistry, immunofluorescence, and radioligand imaging Devise new techniques around tissue-based biomarkers to advance drug development and early discovery programs Conduct in-depth image analysis of whole slide images using established platforms. Provide complex data analysis: report experimental hypotheses, experimental details, summation of raw data, graphs and statistical analysis Supervise the development of multiplex IHC, FIHC and ISH assays to support clinical trials Mentor and train direct or matrixed reports Interface with other line functions, researchers and key stakeholders within and outside the organization Stay updated on the latest developments and trends in the field of Oncology and Radioligand Therapy Present data at internal and external meetings Champion external publications and presentations Deliver high-quality data to impact drug discovery and projects in clinical development Role Requirements: PhD and ideally 2 yrs + postdoctoral/industry experience in Oncology, the Biological Sciences or a related field Must have experience developing singleplex and multiplex immunohistochemistry and immunofluorescence tissue-based assays Proven experience with advanced image analysis using various software tools, including HALO Experience working with cross-functional teams and demonstrated ability to independently drive projects in a matrixed environment Background in radioligand development and autoradiography is a plus *Restrictions on flexible working may apply and will be discussed during interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10022190 Sep 16, 2024 Switzerland Summary -Gerätebediener -Ausführen zugewiesener Fertigungsaufgaben und -tätigkeiten nach Produktionsplan, um die rechtzeitige Produktion des Produkts mit der Qualität und Quantität in Übereinstimmung mit den einschlägigen GMP-, Sicherheits- und Umweltrichtlinien zu ermöglichen. -Service-Operator -Ausführen zugewiesener Fertigungsaufgaben und -tätigkeiten gemäß Produktionsplan in Übereinstimmung mit den einschlägigen GMP-, Sicherheits- und Umweltrichtlinien. Führen Sie routinemäßige operative Support-Aktivitäten nach dem Herstellungsprozess und Zeitplan durch und ermöglichen Sie die zeitnahe Produktion des Produkts mit der Qualität und Quantität -Dokumentationsspezialist Admin Der Dokumentationsspezialist Admin verwaltet die Änderung, Bearbeitung, Verteilung, Überprüfung und Archivierung von GMP-Fertigungsdokumenten und die Ausgabe der Batch-Datensätze, um sie in der Qualität und innerhalb der Fristen an die Produktion zu liefern. Der Dokumentationsspezialist Admin stellt eine Reihe von Verwaltungsaufgaben sicher, die für das ordnungsgemäße Funktionieren des Geräts erforderlich sind. About the Role Ihr V** erantwortungsbereich:** - Kontrollieren der Produkte anhand der Wiegeaufträge - Systemunterstütztes Auswiegen von Hilfs- und Wirkstoffen; Etikettieren der Dispensationsgebinde Auswägen der Restmengen und korrigieren der Gewichtsangaben auf den Gebindeetiketten - Reinigen Dispensationskabine und Einrichtungen gemäss Vorgaben SOP-s - Protokollieren der ausgeführten Dispensationen und Reinigungen Kontrollieren der Leergebinde auf Sauberkeit; Kontrollieren der Produkte auf visuell feststellbare Verunreinigungen, Fremdkörper, usw. Bei Abweichungen vom Sollzustand, Dokumentation und Meldung Einhalten der SOP-s, Hygiene- und Sicherheitsvorschriften gemäss den GSU-Richtlinien Was Sie zur Rolle mitbringen: Abgeschlossene Lehre als Laborant, bevorzugt Pharma/Chemikant, aus der Lebensmittelindustrie oder gleichwertige Ausbildung Erfahrung im Bereich Materialentnahmen von chemischer/pharmazeutischer Rohstoffverarbeitung von Vorteil Erfahrung im Bereich Lager und Logistik, Qualitätskontrolle, Reinraumtätigkeiten im pharmazeutischen GMP-Umfeld Deutsch in Wort und Schrift, Englisch Grundkenntnisse Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an diversity.inclusion_ch@novartis.com und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en\_US/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Operations Business Unit Innovative Medicines Location Switzerland Site Stein Aargau Company / Legal Entity C046 (FCRS = CH028) Novartis Pharma Stein AG Functional Area Technical Operations Job Type Full time Employment Type Befristet (Befristet) Shift Work No

Job ID REQ-10025437 Oct 17, 2024 Switzerland Summary Als Automatiker übernehmen Sie die Wartung und Instandhaltung gemäss Instandhaltungs-Plan und sind für Störungsbehebung und verhindern von Anlagenstillständen zuständig. About the Role Ihre Verantwortungsbereich: Wartung und Instandhaltung gemäss Instandhaltungs-Plan. Sie sind in erster Linie zuständig für die technische Verfügbarkeit aller Anlagen bzw. Nebenaggregate inklusive der vorbeugenden Instandhaltung (TPM). Diese Tätigkeiten beinhalten spezielle GMP-Anforderungen und sind gemäss den gültigen Richtlinien durchzuführen Störungsbehebung und verhindern von Anlagenstillständen. Frühzeitiges Erkennen von Problemen und Einleitung der ersten Schritte zur Behebung Technische Bereitstellung der Anlagen gemäss Produktionsauftrag und Unterstützung von Projektarbeiten und Engineering Gruppe Kennt die Prozessabläufe in seinem Arbeitsbereich im Detail Pflege von Dokumentationen. Ordnungsgemässe Durchführung von Schichtübergaben und einwandfreie Dokumentation sämtlicher Aktivitäten (Logbücher, SAP). Konsequente Verfolgung der Einhaltung von GxP, Daten-Integrität, GSU-Richtlinien und SOP-s Was Sie zur Rolle mitbringen: Abgeschlossene Berufsausbildung zum Automatiker (oder vergleichbar) Erfahrungen in Mess- und Regeltechnik, Siemens (S7 und TIA), Scada-Systeme, Bildverarbeitung mit Kamerasystemen, PC-Kenntnisse (Hard- und Software) Pneumatische und hydraulische Grundkenntnisse GMP- und GSU-Kenntnisse sowie Erfahrung im Arbeiten nach SOP-s Deutsch (fliessend), Englisch (Grundkenntnisse) Von Vorteil sind Berufserfahrung in der Pharma-, Kosmetik- oder Nahrungsmittel-Industrie Warum Novartis? Unser Ziel ist es, die Medizin neu zu erfinden, um das Leben der Menschen zu verbessern und zu verlängern. Unsere Vision ist es, das angesehenste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie können wir das erreichen? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns jeden Tag antreiben, unsere Ziele zu erreichen. Werde Teil dieser Mission und schließe dich uns an! Erfahre hier mehr: https://www.novartis.com/about/strategy/people-and-culture Was du erhältst: Alles, was du über unsere Leistungen und Prämien wissen musst, findest du im Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Engagement für Vielfalt und Inklusion: Novartis setzt sich für die Schaffung eines hervorragenden, integrativen Arbeitsumfelds und vielfältiger Teams ein, die die Patienten und Gemeinschaften, denen wir dienen, repräsentieren. Barrierefreiheit und Anpassungen Novartis ist bestrebt, mit allen Personen zusammenzuarbeiten und angemessene Vorkehrungen für sie zu treffen. Wenn du aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigst oder detailliertere Informationen über die wesentlichen Funktionen einer Position erhalten möchtest, sende bitte eine E-Mail an diversity.inclusion_ch@novartis.com und teile uns die Art deines Anliegens und deine Kontaktinformationen mit. Bitte gib in deiner Nachricht die Nummer der Stellenausschreibung an. Tritt unserem Novartis-Netzwerk bei: Wenn diese Stelle nicht zu deiner Erfahrung oder deinen Karrierezielen passt, du aber auf dem Laufenden bleiben und mehr über Novartis und unsere Karrieremöglichkeiten erfahren möchtest, tritt hier dem Novartis-Netzwerk bei: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Operations Business Unit Innovative Medicines Location Switzerland Site Stein Aargau Company / Legal Entity C046 (FCRS = CH028) Novartis Pharma Stein AG Functional Area Technical Operations Job Type Full time Employment Type Regulär Shift Work No

<div class="box" id="inserat-details"><h1>Suche Nebenjob: Waschen, Bügeln, Kochen, Kinderbetreuung uvm.</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorien</div><div class="display-field"><a href="/stellenmarkt">Job-/Stellenmarkt</a> › <a href="/nanny">Nanny/Hausangestellte</a>, <a href="/koch">Koch/Köchin/Hauswirtschaft</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 8048 Zürich Altstetten, Stadtkreis 9, <a href="/zuerich">Kanton Zürich</a><br/>Tüffenwies </div></div></div><div class="description">Grüezi<br/>Ich bin eine 50-jährige Schweizerin auf der Suche nach einem Nebenjob. Pflege Ihre Wäsche, Einkaufen, Kochen, Ferienbetreuung der Wohnung. Kinderbetreuung, Mittagstisch, Büroarbeiten und vieles mehr...<br/>Ich freue mich auf Ihr Angebot.<br/><br/>Herzliche Grüsse<br/><br/>Raum Zürich, Altstetten, Höngg, Schlieren, Grünau, Albisrieden<br/><br/>Stundenlohn Fr. 30.00</div> <div class="toolbar"><ul><li> Inserat 108669 vom 30.09.2024 </li></ul></div></div></div>

<div class="box" id="inserat-details"><h1>Kinderbetreuung zu Hause (Schweizerisches Rotes Kreuz Kanton Schwyz)</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorien</div><div class="display-field"><a href="/kinderbetreuung">Kinderbetreuung</a> › <a href="/babysitter">Babysitter, Babysitting</a>, <a href="/betreuung">Kinderbetreuung Diverse</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 6430 Schwyz, <a href="/schwyz">Kanton Schwyz</a></div></div></div><div class="description">Familien können in Situationen geraten, die sie überfordern. Mit der Kinderbetreuung zu Hause zeigt sich das Rote Kreuz von seiner familiärsten Seite. Verlässlich, schnell und kompetent erweist es sich als fester Rettungsanker, wenn das Familienboot einmal in unsichere Gewässer gerät. Im Mittelpunkt steht dabei immer das Wohlbefinden der Kinder.<br/><br/>Wir organisieren eine qualifizierte Betreuung, die auch für schwierige Situationen ausgebildet ist. Sie ist in der Regel innert weniger Stunden bei Ihnen zu Hause. Es werden Kinder bis zum Alter von 12 Jahren betreut.<br/><br/>Melden Sie sich unter 041 811 75 74 oder ausserhalb Bürozeiten unter 041 811 75 76.<br/><br/>Schweizerisches Rotes Kreuz Kanton Schwyz<br/>Herrengasse 15<br/>6430 Schwyz<br/><br/><a class="contact-link" data-protected-email="CfDJ8EDJWQJ_AGNPiFWQKPQtWBCZ3TqfZA99D9Av7SeNp5jh36fyg7me2hQX2uM3S_XrVguVEMpn-GuegxOebSVK-zbAidDO9slev5O3h7xWxoIx_kb28zLijAAkUxC9Do_cjhRCgcPWsGEPAvFxASrqe2s" href="javascript:;">E-Mail</a><br/><a href="/inserate/105538/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBDbQMgtlRX55dAfyegBltN4b4mbu2eCkRu9oaaz8Wzne6BFlWWpiOlN7rwXiIufLLAzn-i0bUFVKdIa7UojdoMnV_TtdbX4X5ZmSvQDOoOADbmFXhLvEcb3Dkv2DNT8Apk" rel="nofollow" target="_blank">www.srk-schwyz.ch</a></div> <div class="pictures"><img alt="Bild 1: Kinderbetreuung zu Hause (Schweizerisches Rotes Kreuz Kanton Schwyz)" src="/inserate/105538/bilder/1"/></div><div class="toolbar"><ul><li> Inserat 105538 vom 07.10.2024 </li></ul></div></div></div>

<div class="ui-corner-all" id="page"><div class="content"><div class="toolbar"> </div><div class="body"><p></p><div class="button-top"></div><h1 class="ui-corner-all">Messtechniker 100% (m/w)</h1><h2>Aufgaben</h2><p><ul><li>Programmierung und Bedienung der 3D Messmaschinen (wie zB. Mitutoyo) <li>Bedienen des Konturenmessgerät, Handmessmittel und Projektor <li>Durchführen von Eingangs-, Zwischen-, Endkontrollen sowie Erstmusterprüfungen <li>Fehlermeldungen erstellen und bearbeiten<li>Korrekturmassnahmen veranlassen <li>Qualitätsbezogene Abklärungen intern und extern <li>Kontakt mit Kunden und Lieferanten Prüfpläne erstellen</li></li></li></li></li></li></li></ul></p><h2>Anforderungsprofil</h2><p><ul><li>Mechanische Grundausbildung, idealerweise in der spanabhebenden Fertigung <li>Erfahrung in Mess- und Prüfmethodik <li>Gute IT-Kenntnisse (u.a. MS Office), Englischkenntnisse von Vorteil<li>Kommunikative und dienstleistungsorientierte Persönlichkeit <li>Selbständige, exakte und zuverlässige Arbeitsweise</li></li></li></li></li></ul><br/>Haben wir Ihr Interesse geweckt? Dann senden Sie uns noch heute Ihre Bewerbungsunterlagen per Mail.</p><p>Arbeitsort: Raum Toggenburg</p><p>Bereich: Industrie diverse</p><p>Stellenantritt: per sofort</p></div><div class="footer"><ul><li><h3>All in One Personal Ost AG</h3></li><li>Hofwisenstrasse 2, 8260 Stein am Rhein</li><li>Ihr Ansprechpartner: Dmitrij Wartmann </li><li>Tel: +41 52 741 49 49</li><li>Email: E-Mail schreiben </li><li>Ref: 2171-101142-1-1</li></ul></div><div class="button-bottom"></div></div></div>

Job ID REQ-10024679 Oct 08, 2024 Switzerland Summary As Senior Process Expert CGT you will act as subject matter expert for all process-specific issues to ensure execution of processes on time, continuously improving in quality and productivity, performed in compliance to cGMP, SOPs and applicable guidelines and functional standards. Supports processes and standards to maintain and improve existing and to implement new innovative concepts and strategies. About the Role Why join Cell & Gene Therapy? Novartis is pioneering the way in the class of cell and gene treatment and has developed the first CAR-T cell therapy approved for pediatric and young adult patients with relapsed/refractory B-cell acute lymphoblastic leukaemia (ALL). The patient is at the center of the process for CAR-T cell therapy. The process begins with the patient at autologous T-cell collection and ends with the patient at infusion. Key Responsibilities: Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements. Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batch Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment). Support steward for assessment of technical changes and process changes (task manager ACC/PCC). Collect data for ongoing process verification (OPV), support product steward in tracking and evaluation of product performance and implementation of CAPAs. Support the execution of process validations and qualifications, and short-term improvement projects, liaising with all the relevant parties at shop floor to ensure accurate execution. Perform first line evaluation of product and process related issues, perform root-cause investigations (uncritical, major and critical deviations, complaints, OOS, OOE) and implement effective CAPAs. Ensure that technical batches generate sufficient process knowledge by thoroughly testing critical variables. Support technology trainings and education programs for production operators and others. Act as Subject Matter Expert for Audits. Minimum Requirements: Minimum BSc. or MSc. in Biotechnology, Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree with some years of experience in a technical process support role on the shopfloor of GMP manufacturing. Or: PhD in Biotechnology, Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree with less experience in a technical process support role on the shopfloor of GMP manufacturing. Fluent English language skills (written and oral). German language skills are desirable. Experience working in a GMP environment. Knowledge of Cell & Gene topics. Root cause investigation skills. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network : If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Operations Business Unit Innovative Medicines Location Switzerland Site Stein Aargau Company / Legal Entity C046 (FCRS = CH028) Novartis Pharma Stein AG Functional Area Technical Operations Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.