Description
Responsibilities
- Perform manufacturing activities according to cGMP guidelines
- Ensure batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for technical solutions
- Responsible for the planning, the execution and documentation of manufacturing campaigns in the area of mammalian USP/DSP/F&F manufacturing
- Help solve complex deviations by performing investigations and suggesting CAPAs
- Train the operators
- Support the manufacturing site for audits/customers visits
- Participate to validation activities
Your profile
- Master's degree in Life Sciences (e.g. Biotech, Biochemistry, Pharmacy, Process Engineering) or above
- Excellent biotechnology expertise and/or knowledge in biotech engineering, preferable in the area of Mammalian cell culture and/or protein purification
- More than 3 years' experience under a GMP environment
- Able to perform process-related troubleshooting activities and read P&IDs
- You are a hands-on person with a fluent level in German and English