Production QMS Executive/Sr. Executive

Job Purpose To support and maintain Quality Management System (QMS) activities in vaccine manufacturing operations and ensure compliance with GMP and regulatory requirements. Key Responsibilities Manage and review deviations, CAPAs, and change controls. Review Batch Manufacturing Records (BMRs) and production documentation. Ensure compliance with GMP, SOPs, and data integrity requirements. Support investigations and root cause analysis for quality issues. Coordinate document control activities, including SOP preparation and revisions. Participate in internal audits, self-inspections, and regulatory inspections. Monitor training compliance and maintain training records. Track quality metrics and prepare periodic reports. Support risk assessments and continuous improvement initiatives. Work closely with Production, QC, Engineering, and Warehouse teams. Qualification B.Pharm / M.Pharm <B.Sc> / <M.Sc> (Microbiology, Biotechnology, Life Sciences) Equivalent qualification in Pharmacy or Biological Sciences Experience 2 to 8 years of experience in QA/QMS, preferably in Vaccine, Biologics, or Sterile Manufacturing.