Roles & Responsibilities:
• Execute day-to-day ophthalmic (sterile) production activities as per SOPs and GMP
• Operate, monitor, and document manufacturing processes for ophthalmic formulations
• Ensure adherence to aseptic techniques and contamination control practices
• Prepare, review, and maintain Batch Manufacturing Records (BMRs)
• Perform line clearance, equipment cleaning, and changeover activities
• Monitor critical process parameters and report deviations or abnormalities
• Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations
• Ensure compliance with GMP, safety standards, and regulatory guidelines
Qualification:
• B.Pharm / M.Pharm
Experience:
• 3-5 Years of experience in ophthalmic / sterile production
Key Skills:
• Strong knowledge of sterile manufacturing and ophthalmic processes
• Good understanding of GMP and documentation practices
• Hands-on experience in production equipment and cleanroom operations
• Ability to work in a regulated pharmaceutical manufacturing environment
About the Company:
Ajanta Pharma Ltd is a leading pharmaceutical company with a strong global footprint, specializing in quality-driven formulations including ophthalmic products, and committed to international regulatory and GMP standards.