Roles & Responsibilities
• Ensure compliance with cGMP, GxP, EH&S, and regulatory guidelines
• Complete SOP training and perform activities only after proper authorization
• Manufacture and process batches as per BMR under supervision
• Handle and transfer raw materials, semi-finished, bulk, and finished goods
• Operate, clean, and maintain production equipment as per SOPs
• Maintain GMP, hygiene, and cleanliness in production areas
• Perform in-process checks and ensure accurate online documentation
• Report deviations, incidents, and improvement suggestions through QMS
• Conduct line clearance during product or batch changeovers
• Monitor environmental conditions as per BMR and SOP requirements
• Ensure calibration and preventive maintenance of equipment
• Troubleshoot machine and process-related issues
• Manage issuance, retrieval, and destruction of dies, punches, sieves, and bags
• Attend cGMP, safety, hygiene, and on-the-job training programs
• Support yield improvement, cost control, and efficient production operations
• Carry out additional tasks assigned by the Production Head
Qualification
• Diploma in Pharmacy or B.Sc. (Science)
Experience
• 2–5 years of experience in pharmaceutical production
• Hands-on exposure to Granulation, Compression, Coating, and Encapsulation
Skills
• Strong knowledge of GMP and regulatory compliance
• Experience in solid oral dosage manufacturing operations
• Equipment handling, documentation, and troubleshooting skills
• Attention to hygiene, safety, and quality standards
• Team collaboration and effective communication
• Process improvement and problem-solving ability
About the Organisation
Lupin Limited is a leading global pharmaceutical company with a strong presence in branded and generic medicines. With manufacturing facilities that meet international regulatory standards, Lupin is committed to delivering high-quality, affordable healthcare solutions worldwide.
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