QA Specialist – GMP Manufacturing & Cleanroom
Listed on 2026-10-06
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Quality Assurance - QA/QC
Vericel Corporation, a leader in advanced cell therapies, seeks a QA-focused professional for day-to-day batch record review, labeling, archiving, and final product inspection in our Burlington, MA facility.
You'll gown into ISO 7 clean rooms and support release activities on a Tuesday–Saturday or Sunday–Thursday schedule, with some training/monthly relocation to Cambridge. Strong GMP knowledge and Excel skills are required.
Are you ready to take on the QA Specialist I – GMP Manufacturing & Cleanroom role at Vericel® Corporation?
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Burlington, MA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
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