Assistant Production Manager (Oral Solid Dosage Form)

• Supervise day-to-day production activities for Capsules and Dry Syrup sections.
• Ensure adherence to Batch Manufacturing Records (BMR/BPR), SOPs, and cGMP practices.
• Coordinate with QA, QC, Stores, and Maintenance to ensure smooth operations.
• Plan and monitor production schedules, manpower allocation, and material availability.
• Maintain accurate documentation, in-process checks, and production records.
• Ensure equipment calibration, cleaning validation, and line clearance before batches.
• Identify process deviations and support investigation and CAPA implementation.
  
• Support in regulatory audits, internal audits, and documentation readiness.
• Train and supervise operators, ensuring safety and hygiene in the production area.
• Support scale-up and technology transfer of new products in coordination with R&D.

Required Skills & Competencies

• Strong technical knowledge of capsule filling, dry syrup formulation, and granulation processes.
• Understanding of WHO-GMP / Schedule M compliance requirements.

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  Proficiency in documentation, SOP writing, and deviation handling.
• Excellent coordination and team management skills.
• Analytical mindset with attention to detail and process optimization.

Qualifications & Experience

• B.Pharm / M.Pharm / B.Sc / M.Sc in Pharmaceutical Sciences or related field.
• 5–8 years of experience in OSD production (Capsules/Dry Syrup) in a WHO-GMP compliant facility.
• Experience in regulatory audits (WHO, State FDA, etc.) preferred.