Assistant Manager - Production
Job Description:
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Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
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Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
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Monitor production planning, batch scheduling, material requirement, and manpower allocation.
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Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
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Review and ensure timely completion of batch documentation and deviation/incident reports.
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Supervise equipment operation, cleaning, and validation activities.
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Maintain discipline, safety practices, and 5S in the production area.
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Identify process gaps and implement improvements (CAPA, process optimization, yield improvement).
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Train operators and team members on SOPs, safety, and GMP practices.
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Support audits (internal and external) by providing documents and ensuring compliance readiness.
Required Skills: -
B.Pharm / M.Pharm / B.Sc / M.Sc or relevant qualification.
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5–10 years of hands-on experience in formulation production (OSD / Liquid / Injectable – specify).
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Strong knowledge of machines like RMG, FBP, Compression, Coating, Blister/Strip packing (as per plant type).
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Excellent understanding of GMP, documentation, and regulatory standards.
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Strong leadership, communication, and team-handling skills.
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Ability to manage multiple batches and meet production targets.
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.