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Production In-Charge - Pharmaceutical API Intermediates Manufacturing

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Production In-Charge - Pharmaceutical API Intermediates Manufacturing

SVR Drugs And Intermediates

Production In-Charge - Pharmaceutical API Intermediates Manufacturing

Skills

Testing & QAProcess ImprovementCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Bengaluru, Karnataka, India

Work mode:

Onsite

Published on:

14 August 2026

What they need


Production In-Charge Pharmaceutical API Intermediates Manufacturing

Experience: 5+ Years
Industry: Pharmaceutical API Intermediates / Bulk Drug Manufacturing
Location: Kadechur, Karnataka

Job Description:

We are looking for an experienced Production In-Charge with 5+ years of relevant experience in pharmaceutical API intermediates / bulk drug manufacturing. The candidate will be responsible for managing day-to-day production activities, ensuring adherence to approved manufacturing procedures, cGMP requirements, safety standards, production schedules, and quality requirements.

Key Responsibilities

  • Plan and supervise daily production activities.
  • Execute batches as per BMRs and SOPs.
  • Monitor production processes and batch parameters.
  • Manage production manpower and shift activities.
  • Monitor batch yield and material consumption.
  • Ensure proper production documentation and records.
  • Coordinate with QA, QC, Warehouse, and Engineering.
  • Handle production-related deviations and investigations.
  • Ensure compliance with cGMP and safety requirements.
  • Maintain production areas and equipment standards.
  • Support validation, trials, and process improvement activities.
  • Ensure production targets are achieved on time.

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