Quality Assurance Inspector - III
Job Responsibilities:
- Independently review and approve GMP investigations within the Andover biopharma manufacturing facility.
- Ensure non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated and compliant with cGMP regulations, site, and global procedures.
- Support product quality, patient safety, and timely batch disposition.
- Partner with cross-functional teams including Manufacturing, Engineering, and Quality Control.
- Provide objective QA oversight and support during regulatory inspections and audits.
Skills:
- Strong critical thinking and analytical abilities.
- Clear and effective written communication.
- Objective QA oversight and inspection readiness.
- Experience with quality systems; Vault QMS experience is a plus.
Education/Experience:
- High school diploma or GED required; associate or bachelor’s degree preferred.
- 5–7 years of experience in quality assurance or inspection roles.
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