As a Process Development Scientist, you will play a key role in the development, optimization, and industrialization of pharmaceutical production processes including GMP activities. You will collaborate closely with Clinical Manufacturing and QC teams to support new therapeutic developments and ensure appropriate and robust quality control.
Process Development & Industrialization:
- Design, test, and validate manufacturing processes and equipment.
- Schedule, supervise and perform activities during development and validation phases according to appropriate protocol and guidelines.
- Manage planning and material requirements to perform activities in due time.
- Maintain accurate documentation and traceability of manufacturing data.
- Write protocols and reports for development and validation studies.
- Perform technology transfer in tight collaboration with the operational departments if required.
Work with the Quality Assurance department on SOP, protocol and report.
- Bachelor or Master in Biological Sciences or related field.
- Minimum 2 years of experience with cell culture techniques and associated aseptic environment.
- Be part of a collaborative and international team, yet in an SME setting
- Health insurance, Meal vouchers, Training and development programs