QA Associate: GMP & Batch Record Specialist
Listed on 2026-10-09
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Quality Assurance - QA/QC
Production QC/QA, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Actalent is seeking a QA Associate in Clinton, IN to review data supporting product and packaging quality. You will ensure compliance with cGMPs, write and revise SOPs, and interact with QC and Material Control to support batch releases.
The role focuses on batch records, COAs, and QA documentation, with a 7:30 am–4:00 pm, Monday–Friday schedule in a fully onsite manufacturing environment.
We invite applications for the QA Associate: GMP & Batch Record Specialist position located in MI, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the QA Associate: GMP & Batch Record Specialist role in the description above.
We appreciate your interest in this position.
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