Company Introduction
G.S. Pharmbutor Private Limited manufactures pharmaceutical formulations for regulated and domestic markets.
Core Responsibilities
- Review completed batch records using approved master documents and QA checklists.
- Check cleaning records for equipment and utilities against validated formats.
- Inspect line clearance sheets collected from production areas.
- Log change control forms into quality registers maintained at site.
- File completed audit documents in controlled quality archives.
- Verify calibration labels affixed on laboratory and plant equipment.
Skills & Technical Exposure
- Batch Manufacturing Records and Batch Packaging Records.
- Quality Management System documentation.
- Change control and CAPA registers.
- Calibration status labels.
- Internal audit checklists.
- APQR documentation files.
Experience Context
- Work is performed inside pharmaceutical manufacturing quality offices.
- Handles documentation from multiple commercial batches daily.
- Absence of this role results in unreleased batches and audit gaps.
How to Apply
Email your details to plant.bm@gspharmbutor.com