Description
The role supports and executes qualification of QC laboratory equipment in compliance with cGMP regulations and corporate quality policies. Responsibilities include defining qualification requirements, authoring and executing qualification protocols, coordinating with laboratory personnel and vendors, identifying compliance gaps, and supporting continuous improvement. The position requires a BS/BA degree, pharmaceutical or biopharmaceutical experience, cGMP knowledge, and preferably at least two years of validation or equipment qualification experience. It is scheduled Monday through Friday from 8:00 a.m. to 4:00 p.m., including an unpaid 30-minute lunch, and is five days onsite.
