Role & Responsibilities:

- Prepare, review, and issue controlled copies of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Handle Change Control, Deviation, CAPA, and Investigation activities on the shop floor.
- Prepare and review Standard Operating Procedures (SOPs) and all formats related to manufacturing and packing operations.
- Prepare and control validation protocols and participate in process validation activities.
- Perform in-process monitoring during Dispensing, Granulation, Compression, Coating, and Hard Gelatin Capsule Filling operations.
- Conduct in-process monitoring during packing operations to ensure compliance with specifications.
- Perform Swab and Rinse sampling as per cleaning validation protocols.
- Inspect packing goods for physical attribute evaluation before and after final packing completion.
- Conduct finished product sampling and review of batch records.
- Perform in-process and validation sampling as per approved protocols.




- Calibrate instruments such as Disintegration Tester (DT), Friability Tester, Hardness Tester, and Weighing Balance as per schedule.
- Carry out validation batch sampling according to process validation protocols.
- Ensure in-process controls are effectively performed during manufacturing and that results meet quality standards.
- Review BMRs, logbooks, in-process formats, and other online documentation for accuracy and completeness.
- Conduct cleaning validation sampling and documentation as per approved protocols.

Required Candidate Profile:

- Qualification: B. Pharma / M. Pharma
- Experience: Minimum 1–2 years in pharmaceutical manufacturing (OSD preferred).
- Gender: Male candidates preferred.
- Robust knowledge of GMP, process validation, and in-process quality checks.

📌 Assistant Executive (Una)
🏢 Stanford Laboratories
📍 Una