L 5 - Stability Testing/Analytical Method Development/Process Validation

About the role

The role requires strong leadership to manage the laboratory team, maintain robust analytical practices, and support timely release of products.

What you'll do

• Supervise and manage daily Quality Control activities for raw materials, packaging materials, intermediates, and finished products
• Ensure adherence to GLP, cGMP, and regulatory requirements (e.g., USFDA, WHO-GMP, EU, etc.)
• Review and approve analytical data, specifications, and COAs
• Oversee method validation, method transfer, and stability studies as per protocols
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results and implement corrective and preventive actions (CAPA)

What you need

• 10–12 years in quality assurance & testing
• Chemistry
• GMP
• GLP
• HPLC
• SOP writing
• M.Sc or B.Pharm or M.Pharm

What you get

• ₹8 L–₹10 L a year