Quality Assurance Specialist, GMP & Batch Records
Listed on 2026-10-15
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Quality Assurance - QA/QC
Data Analyst
Actalent is seeking a Quality Associate in Fort Dodge, IA to join the QA Release Group and Process Team. You will review batch records and related technical docs to ensure regulatory compliance with USDA, FDA, and EU standards, while providing real-time QA guidance to production staff.
The role requires 1–2 years in a GMP-regulated environment and hands-on experience with batch records, SOPs, and quality investigations. It’s a contract-to-hire, onsite position offering 40 hours per week.
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This posting is for the Quality Assurance Specialist, GMP & Batch Records role at Actalent, based in Fort Dodge, IA, United States.
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