Executive - Packing QMS

Role & Responsibilities:
• Raise, coordinate, and obtain approval for UPD, PD, and change control documents from relevant authorities
• Handle LMS-related activities and ensure timely completion
• Organize and participate in Cross Functional Team (CFT) meetings related to QMS
• Receive market complaints and ensure timely closure in coordination with CFT teams
• Review and arrange all GMP documentation including formats, logs, and records
• Prepare annual calibration schedules and ensure timely completion
• Implement, monitor, and close CAPA activities within defined timelines
• Ensure completion of scheduled trainings and on-the-job training programs
• Maintain and follow cGMP and GQS guideline requirements
• Handle deviations, change controls, and other GMP compliance documents ensuring timely closure
• Prepare and respond to internal, external, and regulatory authority audits
• Prepare, revise, and archive SOPs as per defined schedules
• Maintain proper archival of all QMS documents and formats
• Update and maintain SOP index for all packing-related SOPs

Qualification:
• B.Pharm (Bachelor of Pharmacy)

Experience:
• 6–8 years of experience in Packing QMS or Quality Assurance within the pharmaceutical industry

Skills:
• QMS & GMP Compliance
• Change Control, Deviation & CAPA Management
• Audit Preparation & Regulatory Compliance
• Documentation & SOP Management
• LMS & Training Coordination
• Cross-functional Collaboration
• Attention to Detail & Time Management

About the Company:
Sun Pharma Laboratories Ltd is a leading global pharmaceutical company committed to quality, innovation, and compliance, offering a collaborative environment where employees grow, take ownership, and thrive together.