Company Introduction
Amgis Lifescience Ltd is an Indian pharmaceutical manufacturer engaged in producing active pharmaceutical ingredients for domestic and international markets.
Core Responsibilities
- Review batch manufacturing records against approved master documents inside quality areas.
- Inspect production and packing areas using line clearance checklists.
- Verify raw material dispensing records with material issuance documents.
- Examine deviation reports and corrective action records in controlled files.
- Check validation reports and stability study documents before approval filing.
- Maintain archival storage of quality documents in designated record rooms.
Skills and Technical Exposure
- Batch manufacturing record and master formula.
- Deviation report and corrective action form.
- Validation protocol and summary report.
- Stability chamber data records.
- Good Manufacturing Practice documentation.
Experience Context
- Work is carried out within active pharmaceutical ingredient manufacturing plants.
- Daily coverage includes multiple production batches and controlled documents.
- Without this role, batch release and compliance documentation halt.
How to Apply
hrd@amgislifescience.com
