Company Introduction
Bliss GVS Pharma Ltd maintains validated systems for formulation manufacturing and regulatory compliance.
Core Responsibilities
- Review completed batch manufacturing records against approved master files.
- Check validation protocols and summarize results in validation reports.
- Inspect production and packing areas using line clearance formats.
- Verify investigation and change control documents before archival.
- Update quality compliance trackers and validation logs.
Skills & Technical Exposure
- Batch manufacturing records
- Validation protocols and reports
- Line clearance documents
- Change control formats
- Quality compliance trackers
Experience Context
- Works inside formulation manufacturing facilities.
- Supports validation of multiple commercial batches.
- Without this role, batch certification is halted.
How to Apply
chetan.pawar@blissgvs.com
