Sr Executive - Production QMS

About the role

Responsible for documentation, deviation handling, and continuous improvement initiatives to maintain product quality and regulatory compliance.

What you'll do

• QMS Compliance & Documentation
• Prepare, review, and maintain SOPs, Batch Manufacturing Records (BMR), and related production documents
• Ensure timely closure of deviations, change controls, and CAPAs related to production activities
• Maintain compliance with USFDA, MHRA, and other global regulatory standards
• Batch Execution & Monitoring

What you need

• 6–10 yrs of experience
• ISO 9001
• Root cause analysis
• GMP
• SOP writing
• B.Pharm or M.Pharm