Sun Pharma Hiring Senior Executive - Production QMS Supervisor

Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.

Post : Senior Executive

Job Description
• Manage Deviation and Investigation processes across manufacturing operations, including planned/unplanned deviations, OOS (Out of Specification), OOT (Out of Trend), and market complaints.
• Drive root cause investigations and ensure timely closure of all quality events in compliance with regulatory expectations.
• CAPA (Corrective and Preventive Actions) implementation in collaboration with cross-functional teams (CFTs), ensuring proper implementation and effectiveness monitoring.
• Prepare and analyze trend reports for deviations, OOS, OOT, and complaints to identify recurring issues and systemic gaps.
• Ensure strict adherence to Good Documentation Practices (GDP) for all GxP-related records and documentation.
• Perform periodic and random report verification to confirm compliance with quality standards and procedures.
• Utilize SAP systems for retrieval and assessment of data related to raw materials, packing materials, semi-finished goods (SFG), and finished goods (FG) for QMS investigations.
• Ensure compliance with cGMP, regulatory guidelines, and internal quality standards at all times.
• Maintain accurate and up-to-date records in quality management systems and trackers for deviations, CAPA, change controls, and investigations.

• Collaborate effectively with QA, QC, Production, Maintenance, Engineering, and HR departments to ensure seamless execution of QMS processes.
• Facilitate cross-functional meetings for investigation closure, CAPA implementation, and continuous improvement initiatives.
• Coordinate and monitor training programs related to QMS, including both classroom and electronic systems (LMS).
• Ensure timely completion of QMS-related training by employees and maintain proper training records.
• Execute track-wise activities (e.g., deviations, change controls) and ensure timely updates in relevant systems.
• Support internal and external audits, regulatory inspections, and ensure timely closure of audit observations.
• To maintain hygienic practices like no eating, no chewing, no smoking, no storage of food in manufacturing area, no self-medication and good sanitation practices etc.
• Adheres to all cGMPs, compliance/regulatory mandates and quality requirements.
• Provide guidance and direction to team members on QMS processes and compliance expectations.
• Assists in the identification and implementation of continuous improvement opportunities.

Additional Information
Educational Qualification : B.Pharma / M.Pharma
Experience : 7+ years
Location : Jammu
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 20th October 2026