This laboratory position will support activities associated with routine in-process testing, Certificate of Analysis (COA) release testing, and stability program support for biologics. The position will also oversee laboratory investigations, identify and implement CAPAs, and manage analytical method lifecycle activities.
Requirements
- Bachelor's, Master's, or Ph.D. in Biology, Chemistry, Biochemistry, or a related scientific field
- Minimum of 10 years of direct, hands-on experience in a GMP Quality Control laboratory supporting biologics
- Deep technical proficiency with HPLC, ELISA, capillary electrophoresis, and compendial testing
- Strong background in laboratory investigations, OOS management, and CAPA implementation
Benefits
- Health insurance
- Retirement plan
- Paid time off