Company Introduction
Mangalam Drugs & Organic Ltd manufactures active pharmaceutical ingredients with integrated production and quality systems.
Core Responsibilities
- Review batch manufacturing records and attach completed checklists with approved master documents.
- Verify IPQA sheets by physically checking line clearance tags and area status boards.
- Inspect filled and packed material against approved specifications using sampling plans.
- Log document movement in controlled registers and file records in designated cabinets.
- Check equipment cleaning records against cleaning schedules and usage logs.
- Prepare dispatch documentation by cross-verifying batch numbers and release notes.
Skills & Technical Exposure
- Batch Manufacturing Records, BMR review checklists, and release notes.
- In-process quality assurance formats and line clearance documents.
- Sampling plans and finished goods inspection records.
- Document control registers and archival systems.
- Cleaning validation records and equipment logbooks.
Experience Context
- Work is performed inside API manufacturing plants and controlled documentation rooms.
- Daily coverage may include multiple batches progressing through production and dispatch.
- Without this role, batch release, dispatch readiness, and compliance records remain pending.
How to Apply
kpandey@mangalamdrugs.com