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Quality Assurance Manager

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Meet Life Sciences
Full Time position
Listed on 2026-02-16
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, QA Specialist / Manager
  • Manufacturing / Production
    QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

The QA Manager serves as the Quality Assurance representative for commercial finished goods and external manufacturing partners. This role oversees quality activities related to finished goods assembly, labeling, packaging, and serialization to ensure compliance with internal standards and global regulatory requirements. The position partners closely with contract manufacturers and internal stakeholders to support reliable, compliant commercial supply.

Responsibilities
  • Act as the QA representative for commercial finished goods and external manufacturing partners.
  • Represent Finished Goods Quality Operations at internal meetings and with contract manufacturers supporting commercial production.
  • Oversee quality aspects of finished goods specifications, qualification and validation activities, artwork, labeling, serialization, and packaging operations.
  • Review and approve manufacturing and labeling documentation, including BOMs, MPRs, product specifications, and variable data.
  • Ensure compliant archival of manufacturing partner documentation within the document management system.
  • Manage quality records such as deviations, CAPAs, change controls, serialization excursions, and issue escalations related to finished goods operations.
  • Identify and recommend continuous improvement initiatives to proactively mitigate risk and support business needs.
Qualifications
  • Bachelor’s degree in life sciences, engineering, or a related field.
  • Minimum of 5 years of experience within the pharmaceutical or biopharmaceutical industry.
  • Hands-on experience with finished goods assembly, labeling, and packaging at external manufacturing sites.
  • Experience leading or supporting root cause analysis, investigations, and effective corrective actions.
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