Manufacturing ​/ Production Associate, Pharmaceutical Manufacturing

Purpose To facilitate the smooth and compliant transfer of pharmaceutical formulations from R&D to manufacturing, ensuring scalability, consistency, and regulatory compliance for successful product commercialization. Position / Job Title Associate/ Officer Department Technology Transfer Reporting To Assistant Manager Location Ambernath Years of Experience 1-2 Years Dosage Form Solid Orals and / or Nasal

Job Responsibilities / Deliverables
1. Documentation Preparation

Preparation of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for Trial batch and exhibit batches.
Compilation of data for Process Evaluation Report (PER) and Hold Time Study Report (HTSR).

2. Batch Execution & Monitoring

Coordinate and monitor scale-up, exhibit, and process validation batches at the manufacturing site.
Ensure all process parameters, in-process checks, and critical control points are followed as per approved BMRs and protocols.

3. Coordination & Cross-Functional Support

Communicate necessary information to CFTs (QA, QC, FD etc.) whenever required.
Arrange all necessary prerequisites, materials, equipment, and utilities prior to batch execution.

Qualifications & Pre-Requisites

M Pharm (Pharmaceutics)
Knowledge of unit operations involved in manufacturing of solid oral dosage forms i.e. Granulation, Blending, Compression, Coating, Capsulation etc. and nasal operations.

Additional notes

Role is expected to work in all shifts.