Onsite GMP Document Control Associate
Listed on 2026-10-11
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Quality Assurance - QA/QC
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Administrative/Clerical
Hire Life Science seeks an Admin/Document Control Specialist for our fully onsite Rhode Island site. You will maintain all required GMP documentation under Quality Management with coaching from the Document Management Subject Matter Expert.
This role focuses on accurate record-keeping and strict adherence to GMP practices. Responsibilities emphasize document control within the GMP framework, ensuring compliance with the Quality System and supporting admin operations during standard hours at the RI
We would love to welcome a new Onsite GMP Document Control Associate to our group in West Greenwich, RI, United States.
The advertised compensation is 42.000 - 52.000.
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 Onsite GMP Document Control Associate role in the description above.
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