Job Description
Labcorp is looking for an onsite **GMP QA Specialist** for our new CMC facility in Mechelen, Belgium.
**Job Responsibilities:**
+ 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.).
+ Monitors, ...
**Job Responsibilities:**
+ 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.).
+ Monitors, ...