Pharma QA Specialist — GMP, Batch Release & Compliance
Listed on 2026-10-06
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Astek in Zebulon, NC is hiring a QA Specialist to support quality and compliance for Investigational Medicinal Products distributed worldwide. This is a full-time, on-site role (first shift, 8:00 am to 5:00 pm).
The role requires reviewing GMP documentation, managing QMS records, and supporting regulatory inspections. Strong attention to detail and excellent communication are essential.
Join us at Astek as our next Pharma QA Specialist — GMP, Batch Release & Compliance in Zebulon, NC, United States.
All applications are reviewed carefully by our team.
The position is based in Zebulon, NC, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 70..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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