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Participation in projects to ensure facilities, utilities, equipment and computer systems are appropriately validated & qualified, including review and approval of key validation deliverables. Review of metrology methods and specifications for accuracy / relevance and compliance with appropriate quality standards Participates in and approves Quality Related Issue Resolutions, Corrective / Preventive Actions (CAPA), Change Controls, Vendor Management and Complaint Handling, Continual Improvement, as appropriate. Facilitation of root cause investigations / risk assessments and engineering solutions to address process quality issues The review and approval of pharmaceutical GMP studies: Providing regulatory review of study related documentation (e.g. methods, protocols, reports, certificates of analysis, etc.). <...
About the Role
Labcorp is looking for an onsite GMP QA Specialist for our new CMC facility in Mechelen, Belgium.
Job Responsibilities:
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