Cincinnati, Ohio
•
Today
Job Summary: - Support validation and commissioning/qualification/validation (CQV) activities onsite for sterile manufacturing and fill/finish operations. - Execute hands-on OQ/PQ (Operational/Performance Qualification) protocols and equipment qualification in a GMP-regulated environment. - Prepare and manage GMP documentation, including protocol execution, discrepancy/deviation resolution, and qualification deliverables. - Work independently and efficiently in a fast-paced, project-driven
Easy Apply
Third Party, Contract
$50 - $60











