Plan and execute tasks related to the preparation of laboratory aliquots in the area of stability, release and reference sample management at the site level
Performing/organising GMP aliquoting (laboratory "bulk" and analytical samples in mg/g range)
Work in accordance with relevant SOPs, GMP, GLP, QM, HSE, ISRM & company guidelines
Manage inventory (electronic and physical) on behalf of the analytical laboratory in centralised facilities
Deliver to appropriate quality standards, ensuring compliance of systems, equipment and processes
Utilise complex tools/equipment, laboratory automation tools and specialised facilities
Preparation of raw data documents for delivery to internal and/or external customers
Review and/or approve documents within own area of responsibility in accordance with current processes
Profile
Education: Minimum: Completed vocational training in (e.g. pharmaceutical development/logistics in GMP) or equivalent
Languages: Fluent in German (oral and written) and basic knowledge of English (oral and written)
Successful work experience in analytical development
Good knowledge of software and computer tools
Mastery of quality principles (GMP, ALCOA+)
Good organisational skills and ability to work independently