Pharm'Up 
Sun Pharma is seeking an experienced pharmaceutical professional for the role of Senior Executive – Production Quality Management System (QMS) Supervisor at its Jammu manufacturing plant. The position focuses on overseeing manufacturing deviations, root cause analyses, CAPA management, and regulatory compliance.
Position Summary
- Designation: Senior Executive (Production QMS Supervisor)
- Company: Sun Pharma
- Location: Jammu
- Functional Area: Production / Quality Management Systems (QMS)
- Application Deadline: October 20, 2026
Core Responsibilities
- Investigations & Event Management: Lead end-to-end investigations for planned and unplanned deviations, Out of Specification (OOS), Out of Trend (OOT) occurrences, and market complaints across production areas.
- CAPA Execution: Formulate, implement, and track Corrective and Preventive Actions (CAPA) with cross-functional teams (CFT) while ensuring effectiveness monitoring.
- Trend Analysis: Prepare periodic trend reports for recurring deviations, OOS, and complaints to identify and address systemic gaps.
- SAP & Data Systems: Utilize SAP to track and review data across raw materials, packaging materials, semi-finished goods (SFG), and finished products during QMS assessments.
- Documentation & Compliance: Enforce Good Documentation Practices (GDP) and strict cGMP protocols; maintain up-to-date tracking for change controls, investigations, and audit trails.
- Audits & Inspection Readiness: Support internal, external, and regulatory agency inspections, ensuring swift remediation and closure of audit observations.
- Training & Mentorship: Oversee classroom and electronic LMS training for manufacturing personnel regarding QMS compliance and Good Sanitation/Hygienic practices.
Eligibility & Candidate Profile
- Education: B.Pharm or M.Pharm
- Experience: 7+ years of dedicated experience in Production QMS or Quality Assurance within a regulated pharmaceutical formulation plant
- Key Skills: Root Cause Analysis (RCA), CAPA effectiveness checks, SAP system operations, GDP/cGMP enforcement, and cross-functional team leadership
About the Author
