GMP Compliance Documentation Specialist

A pharmaceutical company is seeking a qualified candidate for a position involving the review of manufacturing documentation. The role includes ensuring compliance with cGMP, conducting batch record reviews, and maintaining documentation standards. Ideal candidates will possess strong MS Office skills, attention to detail, and the ability to work independently in a fast-paced environment. An Associate's degree or relevant experience in manufacturing quality documentation is required.

Flexible work hours and the ability to lift 30 pounds are also necessary.
Join us at Planet Pharma as our next GMP Compliance Documentation Specialist in IL, United States. This posting is for the GMP Compliance Documentation Specialist role at Planet Pharma, based in IL, United States. We are looking to fill the GMP Compliance Documentation Specialist position at Planet Pharma in IL, United States.