• Perform plant troubleshooting and process optimization in coordination with Production teams
• Investigate and close OOS/OOT cases; execute DOE and implement CAPA
• Develop and implement salvage processes for non-conforming batches
• Prepare and submit PDRs and technical reports to QA
• Participate in Plant CFT meetings and provide technical inputs
• Conduct laboratory trials to resolve plant issues and share technical data
• Ensure documentation compliance with GLP, GMP, and cGMP guidelines
• Participate in continuous training, safety programs, and technical skill development
• M.Sc in Chemistry / Pharmaceutical Sciences or related discipline
• 1–3 years of experience in Process Technology / Manufacturing / Technical Services
• Exposure to pharmaceutical plant operations preferred
• Strong knowledge of GMP, cGMP, and GLP requirements
• Hands-on experience with OOS/OOT investigations, DOE, and CAPA
• Good documentation and report-writing skills
• Strong analytical and problem-solving abilities
• Effective communication and cross-functional coordination skills
Cadila Pharmaceuticals is one of India’s leading pharmaceutical manufacturers with a strong presence across domestic and international markets. Known for its focus on quality, innovation, and patient-centric solutions, Cadila offers robust opportunities for professionals to grow in pharmaceutical manufacturing, process technology, and GMP-driven operations through hands-on exposure and cross-functional collaboration.
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