We are looking for an experienced DGM – Liquid Oral Manufacturing to lead end-to-end manufacturing operations for liquid oral products. The role will be responsible for production, GMP compliance, technology transfer, process optimization, operational excellence, and team management.
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Lead end-to-end liquid oral manufacturing operations, including dispensing, syrup preparation, compounding, filling, and packing.
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Ensure compliance with GMP/cGMP, SOPs, quality, safety, and regulatory requirements.
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Drive production planning, capacity utilization, productivity, yield, and operational efficiency.
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Lead technology transfer, scale-up, commercialization, and process validation activities.
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Drive process optimization, continuous improvement, and cost-reduction initiatives.
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Coordinate with QA, QC, R&D, Engineering, Regulatory, Maintenance, and Supply Chain teams.
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Review and manage batch records, SOPs, deviations, CAPA, and change controls.
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Ensure effective investigation and closure of manufacturing-related deviations, OOS/OOT, and quality issues.
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Monitor key manufacturing KPIs such as OEE, yield, productivity, rejection, downtime, and batch cycle time.
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Lead, mentor, and develop manufacturing teams while ensuring effective manpower planning and training.
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Support regulatory inspections and customer audits related to manufacturing.
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Maintain high standards of EHS, housekeeping, compliance, and manufacturing excellence.
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B.Tech / M.Tech / B.Pharm / M.Pharm or relevant technical qualification.
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18–25 years of experience in pharmaceutical manufacturing.
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Strong experience in Liquid Oral Manufacturing is preferred.
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Hands-on experience in syrup preparation, compounding, filling, and packaging operations.
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Strong knowledge of GMP/cGMP, validation, technology transfer, scale-up, and commercialization.
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Proven experience in manufacturing leadership and team management.
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Strong problem-solving, decision-making, and cross-functional coordination skills.