Your tasks and responsibilities:

• You are responsible for managing Quality Control activities of CDMO projects for the contract development and manufacturing of active biopharmaceutical ingredients in close cooperation with the Project Manager
• Monitoring and coordination of analytical project activities in all planning and implementation phases, especially with regards to deliverables (e.g. method development and validation activities, stability studies, routine batch testing, reference standard characterization)
• First point of contact for customers in analytical project-related questions
• You will work closely with the analytical departments, process development, manufacturing and quality assurance at our three locations in Germany

Your competences:

• You have successfully completed a university degree (Master or comparable) in biology, biochemistry, biotechnology or a related field
• You have several years of professional experience within Quality Control in the pharmaceutical industry in a GMP environment
• You preferably have knowledge in the field of protein analytical and molecular biological methods, e.g. capillary electrophoretic methods, HPLC, q PCR, pharmacopoeia methods
• You have keen interest in successfully managing analytical projects in the pharmaceutical and biotechnology industries, have strong communication skills and the ability to work in a team
• Your sense of responsibility is coupled with cross-functional process thinking
• You have excellent written and spoken German and English skills