Batch Record QA Specialist — cGMP & Compliance
Listed on 2026-10-07
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Production QC/QA -
Pharmaceutical
Piper Companies is seeking a Batch Record Review Specialist to review executed batch records and related manufacturing documentation for accuracy, completeness, and compliance with cGMP and regulatory standards. This role supports timely batch disposition and the release of safe, high‑quality biopharmaceutical products.
Responsibilities include verifying records against master batch records, identifying discrepancies, and collaborating with Manufacturing, QC, and Validation to resolve issues
We would love to welcome a new Batch Record QA Specialist — cGMP & Compliance to our organisation in Gaithersburg, MD, United States.
Learn more about the Batch Record QA Specialist — cGMP & Compliance role in the description above.
We appreciate your interest in this position.
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