Packaging cqv engineer
WicklowCpl
...project milestones. Ensure 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 [...]
Contract Type: Freelance
Category Logistics, Transport & Distribution