Company Introduction
Zytex Biotechnology Pvt. Ltd. operates specialized biotechnology and fermentation manufacturing facilities supplying regulated domestic and export markets.
Core Responsibilities
- Review completed batch manufacturing records using printed BMR files and approved reconciliation checklists.
- Verify cleaning records by cross-checking equipment logbooks and validated cleaning status labels.
- Inspect material dispensing areas through physical checks against line clearance forms.
- Approve controlled documents by stamping, signing, and filing master copy registers.
- Track change control notes and closure sheets within QA document control cabinets.
- Observe manufacturing rooms to confirm compliance with gowning SOP displays.
Skills & Technical Exposure
- Batch manufacturing records, validation protocols, and change control formats.
- Document management systems and controlled document registers.
- GMP guidelines, audit checklists, and SOP master lists.
- Deviation notes, CAPA formats, and risk assessment templates.
- Label control logs and document archival files.
Experience Context
- Work takes place inside a fermentation manufacturing unit with controlled access areas.
- Multiple batches run simultaneously across upstream and downstream sections.
- Without QA oversight, batch release stops and regulatory inspections remain unresolved.
How to Apply
hr2.baroda@zytex.com