Title: Quality Assurance Inspector - III
Contract: 01 Year + (Contract with potential to extend)
Location: Andover, MA 01810
Description
Standard hours Mon - Fri start time flexible from 7am- 9am. Teams Interview
Summary
- The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility.
- This role ensures non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated, and compliant with cGMP regulations, site and global procedures.
- The position supports product quality, patient safety, and timely batch disposition while partnering with cross-functional teams including Manufacturing, Engineering, and QC.
- The ideal candidate demonstrates strong critical thinking, clear written communication, and the ability to provide objective QA oversight, including support during regulatory inspections and audits.
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.