L 3 - Quality Assurance

About the role

The General Manager – Quality Assurance (QA) will be responsible for leading and overseeing all QA functions at the pharmaceutical manufacturing site to ensure compliance with cGMP, regulatory guidelines (USFDA, EU, MHRA, TGA, etc.), and company quality standards. The role is pivotal in establishing a robust Quality Management System (QMS), driving a culture of compliance, and ensuring the release of safe and effective pharmaceutical products.

What you'll do

• Lead the QA department to ensure strict adherence to current Good Manufacturing Practices (cGMP)
• Define and implement site-wide QA strategies in line with global quality policies
• Establish robust systems for product quality assurance, documentation, and compliance
• Ensure the site remains audit-ready at all times and leads all external inspections (USFDA, MHRA, EU, WHO, etc.)
• Manage responses and CAPA implementation for regulatory inspections and customer audits

What you need

• 15–20 yrs of experience
• GMP
• Chemistry
• Microbiology
• ISO 9001
• Regulatory affairs
• M.Sc or B.Pharm or M.Pharm

What you get

• ₹30 L–₹35 L a year