Zentiva Group is seeking an Executive QA Documentation professional with 1 to 5 years of experience in Pharma Quality Assurance or Documentation. The ideal candidate should possess strong knowledge of cGMP, GDP, and Quality Systems, with a focus on document control and regulatory compliance
Job Summary
The role involves reviewing and maintaining Master Batch Manufacturing Records to ensure regulatory compliance.
Candidates will prepare, compile, and review Annual Product Quality Reviews in line with regulatory expectations.
The position requires coordinating cGMP training programs and managing archival systems for controlled documents.
Matching Summary
Match Score: 80
Zentiva Group is seeking an Executive QA Documentation professional with 1 to 5 years of experience in Pharma Quality Assurance or Documentation. The ideal candidate should possess strong knowledge of cGMP, GDP, and Quality Systems, with a focus on document control and regulatory compliance.