Senior Quality Lead für Hays (Schweiz) AG in Basel - jobbasel.ch
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Position

      26.09.2026

      Senior Quality Lead

      • Basel
      • Festanstellung 100%

      • Merken
      • drucken
       

      Hays (Schweiz) AG

      Hays (Schweiz) AG

      Senior Quality Lead

      Senior Quality Lead

      (m/f/d)

      Freelance/temporary employment for a project

      Basel

      Start date: asap

      Reference number: 890604/1

      Responsibilities

      • Establish relationships with business stakeholders and lead the development of molecule/product/process/affiliate-level approaches with appropriate measures (CtQ Factors)

      • Analyze quality data to identify trends and risks, providing insights to business partners

      • Lead and perform complex audits and quality assessments

      • Synthesize individual audit issues into systematic conclusions and present findings and associated risks to senior stakeholders, ensuring quality data fulfills regulatory requirements and supports organizational goals

      • Play a lead role in inspection preparation and management as well as providing training to staff and ensuring relevant materials are prepared for regulatory review

      • Lead assigned goals and initiatives and drive the development or revision of PDQ processes

      • Maintain and influence partnerships with senior business stakeholders and PDQ domains

      • Facilitate cross-functional collaboration to ensure quality standards are met globally

      • Expert knowledge in GxP regulations (FDA, EU, ICH guidance) and internal policies

      • Ensure all activities are conducted in compliance with regulatory and company requirements

      Profile

      • Bachelor-s degree or equivalent in a scientific or quality-related field. Advanced degree preferred
      • Significant experience in the pharmaceutical / biotech / medical device industry, including knowledge of the end to end development and operationalisation of products, and the associated GxP regulations and considerations (e.g., GCP,GVP, IVD/MD Regulations)
      • Solid experience in leading GxP audits and managing complex quality projects
      • In-depth knowledge of drug development processes and global regulatory landscapes
      • Good understanding of Information Systems, e.g., audit management and analysis reporting tools
      • Fluency in written and spoken English; bi or multi-lingual skills are desirable
      • Clinical Operations experience or quality function in system validations
      • Leadership and Stakeholder Management: Demonstrates exceptional ability to influence, negotiate, and mentor while effectively managing relationships with diverse stakeholders in global settings
      • Analytical and Strategic Thinking: strong data and digital literacy, with the critical thinking ability to synthesize complex or ambiguous information into clear, actionable insights
      • Execution and Independence: Combines strong organizational and project management skills with the capacity to work effectively-both independently and collaboratively-within international, agile matrix organization

      Benefits

      • Fascinating, innovative environment in an international atmosphere
      • A very renowned company

      Arbeitsort: Basel