A biotech company is seeking a Quality Assurance Professional to join their organization on a contract basis. They have one commercialized drug on the market and are in Phase 3 with another. Specifically, you will be on the QA team responsible for supporting quality activities, reviewing all documentation, ensuring compliance, regularly interacting with cross-functional teams, and more!
Responsibilities:
- Review batch records, product disposition, and ensure compliance to all regulatory and company standards
- Execute CAPAs and resolve quality deviations and investigations
- Ensure documentation is up to standards (change control, protocols, reports, methods, etc.)
- Support internal/external audits
Qualifications:
- 3+ years of experience in Quality in a biotech/pharma/medical device company
- S./M.S in the Life Sciences field
- Experience and knowledge of general compliance and GMP regulations
Benefits
- Health Benefits (Dental, Vision, Medical)
- 401K
- Paid sick days
- Lunch provided twice a week
If interested, please don't hesitate to apply!