Manager

<p> Role: Manager (M2) - Production </p> <p> Location: Pithampur Unit-3 </p> <p> Reports To: Senior Manager / Plant Production Head </p> <p> Experience Required: Min 15 years in Pharmaceutical manufacturing with exposure to regulatory-approved facilities (USFDA, MHRA, EU, etc.). </p> <p> Specialization: Derma, Nasal, Liquid Oral dosage forms </p> <p> Education: B. Pharm / M. Pharm B. E. / B. Tech M. Sc. (Chemistry, Biotechnology, Pharmacy, or related disciplines) </p><p> Key Expectations </p> <p> Production Management Execute manufacturing and filling activities as per plan. Achieve production targets and schedule adherence. Ensure optimum utilization of manpower, equipment, materials, and utilities. Handle SAP, Viva, e BMR/EBR, and PAS-X MES systems. </p><p> Quality &amp; Compliance Ensure compliance with c GMP, Data Integrity, and regulatory requirements. Maintain audit readiness for USFDA, MHRA, EU, WHO, etc. Manage deviations, investigations, CAPA, OOS/OOT, and market complaints. Support validation, qualification, and technology transfer activities. </p><p> Operational Excellence Improve productivity, yield, and cycle times. Drive Lean Manufacturing and Six Sigma initiatives. Reduce manufacturing costs (COGM, CCPC). Lead waste reduction and process optimization projects. </p><p> Equipment &amp; Facility Management Ensure equipment reliability and uptime. Coordinate preventive maintenance and breakdown management. Support automation, digitization, and 21 CFR Part 11 compliance. Participate in expansion and modification projects. </p><p> Safety &amp; EHS Promote zero-accident culture. Conduct risk assessments and incident investigations. Drive safety observations and corrective actions. </p><p> People Leadership Develop production teams through training and coaching. Conduct Gemba, SOP, and capability-building sessions. Manage performance, engagement, and succession planning. </p><p> Major KPIs </p> <p> Safety Zero Lost Time Accidents (LTA) Near-miss reporting and closure Safety observation closure rate </p><p> Quality Right First Time (RFT) Deviation reduction CAPA closure compliance Audit observation management </p><p> Delivery Schedule adherence OTIF manufacturing performance Batch release support timelines </p><p> Cost COGM reduction CCPC reduction Yield improvement Cost-saving projects </p><p> Productivity OEE improvement Throughput enhancement Cycle time reduction Capacity utilization </p><p> People Training compliance Attrition control Succession readiness Employee engagement </p><p> Technical Competencies c GMP &amp; Regulatory Compliance Investigation &amp; CAPA Validation &amp; Qualification Lean Manufacturing &amp; Operational Excellence Data Integrity &amp; 21 CFR Part 11 Risk Management </p><p> Behavioral Competencies Leadership &amp; Team Building Decision Making Problem Solving Stakeholder Management Communication Skills Continuous Improvement Mindset </p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p> <p></p>