Company Introduction
Maya Biotech Pvt. Ltd. operates a dedicated injectable manufacturing facility focused on sterile pharmaceutical products under regulated quality systems.
Core Responsibilities
- Review raw data sheets generated from HPLC, GC, and UV instruments for injectable formulation samples.
- Inspect microbiology culture plates, endotoxin test reports, and sterility test records generated within cleanroom laboratories.
- Verify stability chamber data logs and compiled trend reports for ongoing injectable batches.
- Check method validation files, calibration records, and analytical worksheets against approved specifications.
- Document OOS case files, laboratory investigation notes, and corrective action records in controlled formats.
- Authorize analytical result summaries and batch release quality statements prepared for manufacturing review.
Skills & Technical Exposure
- HPLC systems, UV spectrophotometers, and gas chromatography equipment.
- Sterility testing isolators, laminar airflow benches, and endotoxin testing assemblies.
- Stability chambers with temperature and humidity monitoring systems.
- WHO-GMP compliant quality control documentation formats.
- Laboratory information management systems used for injectable testing data.
Experience Context
- Work is performed inside pharmaceutical quality control laboratories attached to injectable production blocks.
- The role supports multiple sterile batches, stability lots, and routine laboratory sample volumes.
- Without this role, injectable test results remain unverified, stability data remains unchecked, and batch release decisions stall.
How to Apply
hradmin@mayabiotechindia.com