Role & responsibilities

1. Production Operations

- Execute batch manufacturing activities as per BMR and SOPs.

- Dispensing, mixing, granulation, compression, coating, filling, and packing operations (as applicable).

- Ensure proper line clearance before and after batch operations.

- Monitor critical process parameters and maintain in-process controls (IPQC).

- Handle and operate production equipment such as reactors, granulators, blenders, compression machines, coating pans, filling lines, etc.

2. Documentation & Compliance

- Maintain accurate and real-time documentation in BMR/BPR.

- Ensure compliance with FCentral Drugs Standard Control Organization (CDSCO) / GMP guidelines (as applicable to industry).

- Follow Positive Manufacturing Practices (GMP), GLP, and safety standards.





- Assist during internal and external audits.

3. Quality & Process Control

- Coordinate with QA/QC for sampling and in-process testing.

- Identify and report deviations, incidents, and non-conformities.

- Support process validation and scale-up activities.

- Ensure minimum wastage and optimum yield.

Preferred candidate profile

- Knowledge of GMP and regulatory requirements.
- Must have FDA approval in tablets and capsules section.

- Understanding of batch processing and manufacturing operations.

- Basic knowledge of documentation and audit requirements.
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📌 Production Chemist (FDA Approved) (New Delhi)
🏢 Arbro Pharmaceuticals
📍 New Delhi