Packaging cqv engineer
WicklowCpl
...site-wide compliance with current regulatory requirements, including FDA cGMPs, data integrity and applicable validation standards. Compile, review and approve GMP documentation such as VMPs, URSs, DQs, FATs, IOQs, OQs, PQs, and validation reports. Lead and support cleaning validation activities across manufacturing and [...]
Contract Type: Freelance
Category Logistics, Transport & Distribution
30+ days ago in TechSkills