Company Introduction
Zytex Biotechnology Private Limited operates a dedicated fermentation manufacturing facility focused on biotechnology based pharmaceutical production.
Core Responsibilities
- Review batch manufacturing records and verification logs using controlled quality assurance documentation.
- Inspect fermentation vessel cleaning records and sanitation checklists within the manufacturing block.
- Examine raw material release files and vendor qualification documents before material usage.
- Assess in process sampling sheets and laboratory release notes during fermentation batches.
- Approve controlled change notes and stability observation records maintained at the site.
Skills and Technical Exposure
- Batch manufacturing records and quality assurance master files.
- GMP documentation systems used in pharmaceutical plants.
- Change control and document management software.
- Deviation note registers and corrective action records.
- Audit preparation checklists and compliance tracking logs.
Experience Context
- Work is performed inside an active fermentation manufacturing plant handling commercial scale batches.
- Daily interaction involves multiple production lots and concurrent documentation reviews.
- Without this role, controlled records lapse and batch disposition timelines fail.
How to Apply
hr2.baroda@zytex.com