• Handle batch operations in API manufacturing including reactions, distillation, filtration, drying, and charging
• Operate API equipment such as Reactors, Centrifuges, ANFDs, Dryers, and related systems
• Execute production activities in compliance with GMP and safety guidelines
• Prepare and maintain GMP documentation including BMRs, SOPs, and deviation records
• Manage shift activities and shopfloor manpower to meet production targets
• Ensure strict adherence to quality, safety, and regulatory requirements
• Coordinate with cross-functional teams for smooth manufacturing operations
• B.Sc / M.Sc (Chemistry)
• B.Pharm / M.Pharm
• Diploma in Chemical Engineering or related discipline
• 3–8 years of exclusive hands-on experience in API manufacturing
• Strong exposure to bulk drug API batch operations
• Candidates from USFDA / EDQM / ANVISA-approved plants preferred
• Strong knowledge of API batch operations (distillation, filtration, drying, charging)
• Hands-on experience with Reactors, Centrifuges, ANFDs, Dryers
• Good understanding of GMP documentation and deviation handling
• Ability to manage shopfloor activities and production manpower
• Strong problem-solving, coordination, and communication skills
• Date: Friday, 23 January 2026
• Time: 10:00 AM – 4:00 PM
• Venue: Aarti Pharmalabs Ltd – Unit IV, MIDC Tarapur,
Dist. Palghar, Maharashtra
• Note: Only API production experience candidates are suitable
Aarti Pharmalabs Ltd is a leading pharmaceutical company specializing in the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and intermediates. With state-of-the-art facilities approved by USFDA, EU GMP, EDQM, and other global regulators, Aarti Pharmalabs delivers high-quality, compliant solutions to customers worldwide and offers strong long-term career growth for manufacturing professionals.
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