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Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline. 1–5 years of relevant experience in Pharma Quality Assurance / Documentation Strong knowledge of cGMP, GDP, and Quality Systems Hands-on experience with batch documentation and document control systems Good understanding of APQR preparation and regulatory expectations Strong analytical, organizational, and coordination skills Effective communication and cross-functional collaboration abilities Attention to detail and commitment to data integrity Review and maintain Master Batch Manufacturing Records and Master Batch Packing Records to ensure accuracy, regulatory compliance, and alignment with approved specifications and process related changes. Coordinate with Production, QC, and Regulatory Affairs for timely updates and approvals. Prepare, compile, and review Annual Product Quality Reviews (APQRs) in line with regulatory expectations. Support identification of improvement opportunities and follow-up of CAPAs arising from APQR findings. Coordinate and monitor cGMP and quality-related training programs for site personnel. Maintain trainingschedules, records, and effectiveness assessments. Manage the archival room and document storage systems for controlled and historical GMP documents. Ensure secure storage, easy retrieval, retention compliance, and protection against unauthorized access or damage. Support audits and inspections by ensuring availability of archived records.
Executive QA Documentation
onsiteFull-timeNot SpecifiedSalary Undisclosed
About the role
Position Title: Executive QA Documentation
Qualifications & Experience
Educational Qualification
Experience
Skills & Competencies
Key Responsibilities
Review of Master Documents
Annual Product Quality Review (APQR)
cGMP Training Coordination
Archival & Records Retention