Quality Documentation Auditor - Batch Records

medical records specialists

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page mechanical group inc

basic chemical manufacturing pharmaceutical and medicine manufacturing

Mainland, PA

April 1st, 2026

A leading company in the manufacturing sector is seeking a QS Associate I & II – Batch Record Auditor. This role involves managing the life cycle of quality documents and ensuring compliance with cGMP standards in a fast-paced environment. Ideal candidates should hold a Bachelor's degree and have relevant experience in Quality Assurance or Quality Control. The position offers competitive pay with benefits including medical insurance and a retirement plan. J-18808-Ljbffr

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