Quality Assurance Specialist
4 weeks ago
We are currently working with a small to mid-sized biopharmaceutical company focused on Oncology. My client has 6+ clinical trials, with 4 clinical trials being in Phase 2 or further. With multiple sites in the United States and they're looking to add headcount to their San Francisco location. We are looking for a QMS Specialist on a contract basis.
Responsibilities of the role:
- Batch record release
- CAPAs, deviations, and change control
- Manufacturing commercial side experience
- Exposure to drug substance drug products
Qualifications:
- Bachelor's degree in Life Science or related field
- 3+ years of GMP experience
- 3+ years of batch records experience
- 5+ years of pharmaceutical/ biotechnology experience
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