GM

Job Description : GM PHARMA API Manufacturing EUROPE Open to International candidates As a pivotal leader in our production ecosystem, you will drive manufacturing excellence, ensure stringent regulatory compliance, and lead a high-performing team to meet our global supply demands. You will oversee shop-floor operations, optimize production yields, and champion a culture of safety and quality in line with international regulatory standards (USFDA). Operational Leadership: Oversee day-to-day operations of API manufacturing blocks to achieve production targets while optimizing cost, yield, and resource utilization. Regulatory Compliance: Ensure 100% compliance with cGMP, safety (EHS) guidelines, and standard operating procedures. Successfully lead and face regulatory audits (USFDA, EDQM, WHO, etc.). Process Improvement: Drive continuous improvement initiatives to minimize batch cycle times and minimize deviations or market rejections. Team & Resource Management: Mentor, develop, and manage a team of production chemists, Shift incharges fostering a collaborative and high-productivity work culture. Cross-Functional Coordination: Collaborate seamlessly with QA, QC, R&D, Engineering, and Supply Chain teams to ensure smooth technology transfers and uninterrupted production workflows. Education: M.Sc (Chemistry)/ Diploma/B.Tech (Chemical) Experience: 18 to 28 years of hardcore experience in API / Bulk Drug manufacturing. Audit Exposure: Proven track record of successfully handling major international regulatory audits. Skills: Deep technical knowledge of chemical reactions, unit operations, scale-up processes, and advanced automation/equipment handling. Strong strategic thinking, decision-making, and people management skills.

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