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You will be updated with latest job alerts via emailreviewing records and change requests on completeness, consistency, relevance and clarity
providing advice to requesting departments regarding GMP matters and GMP compliance
reviewing documentation relating to raw materials and the release of raw materials
reviewing and preparing batch release documentation
reviewing and approval of QA-controlled documentation (such as SOPs, batch records, working instructions)
support for the development of appropriate Corrective and Preventative Actions (CAPAs) and continuous improvement activities.
Full Time