17 Sep
|
Unichem Laboratories
|
Baddi
17 Sep
Unichem Laboratories
Baddi
Qualification - B Pharma / M Pharma /n Responsibilities /n /n
- Plan, execute, and monitor monthly manufacturing and packing plans across multiple units (Unit I, II & III) to meet market requirements.
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- Ensure strict compliance with cGMP, international regulatory guidelines, and Quality Management System (QMS) requirements.
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- Maintain work discipline, plant safety, housekeeping, and hygiene standards on the shop floor to ensure zero-incident operations.
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- Review and implement Standard Operating Procedures (SOPs), batch manufacturing records, master documents, and compliance records.
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- Investigate process deviations, non-compliances, market complaints, product failures, and Out of Specification (OOS) results.
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- Implement strong Corrective and Preventive Actions (CAPA) to eliminate repeated complaints, rejections, and product recall risks.
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- Authorize and approve artwork, batch allocations, deviations, change controls, and CAPA documents in the plant.
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- Coordinate with cross-functional teams like QA/QC, Engineering, and Sales for validation, preventive maintenance, and dispatch planning.
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- Monitor and control the cost per unit by improving yield, enhancing operational efficiency, and reducing manpower through automation.
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- Handle customer audits, internal audits,
and external regulatory body inspections successfully.
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- Conduct regular technical and cGMP training programs for subordinates, staff, and technicians to develop a multi-skilled team.
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- Manage administrative functions, including recruitment, shift-wise manpower planning, and performance mentoring of the team.
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- Plan, execute, and monitor monthly manufacturing and packing plan of Baddi Unit-1 to meet market requirements
/n /n Desired Skills /n /n
- Should have handled production department in a reputed pharmaceutical organization
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- Solid expertise in pharmaceutical manufacturing processes, technology transfer, and process validation batches.
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- Should have faced regulatory and customer audits.
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- In-depth knowledge of cGMP regulations, international pharma guidelines, and Quality Management Systems (QMS).
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- Proven capability in handling root cause analysis for OOS, deviations, and implementing strong CAPA.
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- Experience in production planning, scheduling, capacity utilization, and shop floor management.
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- Excellent leadership, team management, and mentoring skills to build and develop a second line of leadership.
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- Strong cross-functional coordination and communication skills to handle audits and engineering calibrations.
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📌 Senior Manager - Production (Baddi)
🏢 Unichem Laboratories
📍 Baddi