Offer summary
Qualifications:
Bachelor or Master's degree in chemical, biological or biochemical sciences, 7-10 years of related experience in biopharmaceutical industry, Experience in GMP and aseptic manufacturing environment, Familiarity with AKTA Process skids and single-use consumables, Knowledge of GMP documentation and processes.
Key responsabilities:
- Lead and supervise downstream purification processes in a cGMP environment
- Provide technical direction for purification process development
- Evaluate operating data and adjust processes accordingly
- Prepare and review quality management documents
- Coordinate investigations and corrections during batch execution