Description
The role supports and executes QC laboratory equipment qualification activities under direct supervision while complying with cGMP regulations and client 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 is 100% onsite Monday through Friday from 8:00 AM to 4:00 PM and requires a BS/BA degree, pharmaceutical or biopharmaceutical experience, cGMP knowledge, and preferably at least two years of validation or equipment qualification experience.
