QA Specialist — GMP & FDA Compliance, Batch Review
Listed on 2026-10-11
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Quality Assurance - QA/QC
Production QC/QA, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Adecco US, Inc. is assisting a client in St. Albans, VT in their search for a Quality Assurance Specialist for a long-term assignment on 1st shift, Monday-Friday, 8:00 AM-5:00 PM.
The role focuses on ensuring batch production records, manufacturing operations, and process documentation comply with cGMP requirements, SOPs, FDA regulations, and other quality standards. Ideal candidates will hold a Bachelor’s degree with 0-2 years in a GMP-regulated environment, plus strong attention to detail,
Step into the QA Specialist — GMP & FDA Compliance, Batch Review role at Adecco US, Inc. in St. Albans, VT, United States and grow with us.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in St. Albans, VT, United States.
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