Posted:3 weeks ago|
Platform:
On-site
Full Time
The Production Manager will be responsible for overseeing and managing the entire OSD manufacturing operations, including Granulation, Compression, Coating, and Packing activities. The role requires strong leadership in production planning, compliance, manpower management, and continuous improvement to ensure quality output, productivity, and regulatory readiness.
- Lead and manage end-to-end OSD production operations in alignment with GMP and regulatory standards.
- Plan, schedule, and allocate production batches to ensure timely delivery and adherence to production targets.
- Monitor and control processes in Granulation, Blending, Compression, Coating, and Packing departments.
- Ensure availability of RM/PM, machine readiness, and line clearance before batch execution.
- Coordinate with QA, QC, Warehouse, R&D, Engineering, and Procurement for smooth workflow.
- Ensure strict compliance to SOPs, cGMP, GDP, EHS, and regulatory guidelines at all stages.
- Review and approve BMR/BPR and ensure documentation accuracy.
- Train, guide, and supervise departmental staff, operators, and shift executives.
- Lead deviation investigations, CAPA implementation, and continuous improvement programs.
- Prepare production plans, yield reports, downtime analysis, and MIS reports.
- Drive audit readiness for regulatory inspections (USFDA, WHO, EU GMP, etc.).
- Promote cleanliness, discipline, safety, and compliance culture across production floors.
- Identify and implement strategies to reduce waste, improve efficiency, and optimize cost.
- Education: B.Pharm / M.Pharm / M.Sc or equivalent science background.
- Experience: 1015 years of experience in OSD formulation production, with at least 35 years in a managerial or supervisory role.
- Strong leadership and people management skills.
- In-depth technical knowledge of OSD processes and equipment.
- Excellent planning, problem-solving, and decision-making abilities.
- Good communication and interdepartmental coordination skills.
- Ability to work under pressure and meet production timelines.
- Strong exposure to Regulatory Audits, cGMP, and quality systems in formulation units.
SAIN MEDICAMENTS PVT. LTD
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