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Assistant Production Manager – API Manufacturing

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Onsite

Assistant Production Manager – API Manufacturing

TIVAN SCIENCES PRIVATE LIMITED

Assistant Production Manager – API Manufacturing

Skills

Testing & QARCompliance

25 days ago

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Important information


Contract type:

Permanent

Location:

Rajkot, Gujarat, India

Work mode:

Onsite

Published on:

30 September 2026

What they need


Role Summary

The Assistant Production Manager will support the Production Head in running day-to-day API manufacturing operations. The role owns production planning, shift leadership, cGMP compliance on the shop floor, and continuous improvement in yield, cycle time and cost.

Key Responsibilities

  • Plan and execute monthly production schedules for multi-product API blocks in line with sales and dispatch requirements
  • Lead and allocate manpower across shifts (production officers, chemists, operators) and ensure smooth shift handovers
  • Ensure batches are executed as per approved BMR/BPR and SOPs; review and close batch records on time
  • Handle deviations, investigations, CAPA and change controls in coordination with QA
  • Monitor yields, cycle times, solvent consumption and recovery; drive improvement projects
  • Support scale-up, process validation and technology transfer from R&D to plant
  • Coordinate with QC, QA, Engineering, Stores and Planning for uninterrupted operations
  • Prepare for and participate in WHO-GMP, regulatory and customer audits; ensure timely audit compliance
  • Enforce EHS and process safety practices, including PPE, permit systems and safe handling of hazardous chemicals
  • Train and develop production staff on SOPs, cGMP and safety

Qualifications & Experience

  • M.Sc / B.Sc Chemistry or B.E / B.Tech Chemical Engineering
  • 5–8 years of experience in API / Bulk Drug manufacturing, with at least 2 years in a supervisory or shift in-charge role
  • Hands-on knowledge of reactors, centrifuges, filters, dryers (FBD, VTD, RCVD), distillation and solvent recovery
  • Strong understanding of cGMP, GDP and data integrity (ALCOA+)
  • Exposure to WHO-GMP, EU-GMP or customer audits preferred
  • Good communication in English, Gujarati and Hindi

What We Offer

  • Attractive compensation, commensurate with experience
  • A leadership role in a growing, quality-focused organization
  • Direct exposure to scale-up, new product introductions and regulated-market audits

How to Apply

Apply via LinkedIn or send your CV to [email protected]

Call / WhatsApp: 94288 29803 | www.tivansciences.com

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