Description
The role performs qualification of laboratory equipment in accordance with EQ policies, plans, and procedures; coordinates requirements with laboratory personnel and vendors; authorizes, reviews, and executes qualification protocols; identifies business, quality, and compliance gaps; and supports QC laboratory operations. It requires a BS/BA degree, pharmaceutical or biopharmaceutical experience, knowledge of cGMP or equivalent regulations, and at least two years of validation or equipment-qualification experience, with a standard office work environment.
