Executive QA Documentation

About this role

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Skills you'll use

What you'll do

• Review of Master Documents
• 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.
• Annual Product Quality Review (APQR)
• 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.
• cGMP Training Coordination
• Coordinate and monitor cGMP and quality-related training programs for site personnel.
• Maintain trainingschedules, records, and effectiveness assessments.
• Archival & Records Retention

Who can apply

• Educational Qualification
• Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline.

About Zentiva

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