Onsite GMP QC Systems Consultant | CSV/Validation Lead
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Quality Assurance - QA/QC
Job Description & How to Apply Below
Stark Pharma Solutions Inc in Frankford, DE is seeking a GMP QC Systems Consultant for a 12+ month contract onsite. The ideal candidate will drive the implementation, integration, and validation of Quality Control laboratory systems in a regulated pharma setting.
The role requires 8+ years in GMP environments, hands-on CSV/CSA, GAMP5, IQ/OQ/PQ, and data migration. Collaboration with QA, IT, and laboratory teams is essential to ensure project success and regulatory compliance.
This role is for the Onsite GMP QC Systems Consultant | CSV/Validation Lead role at Stark Pharma Solutions Inc.
We are seeking a motivated Onsite GMP QC Systems Consultant | CSV/Validation Lead to join Stark Pharma Solutions Inc in Frankford, DE, United States.
Consider building your career as a Onsite GMP QC Systems Consultant | CSV/Validation Lead at Stark Pharma Solutions Inc.
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