Company Introduction
BDR Pharmaceuticals is an India based pharmaceutical manufacturer engaged in research driven development and large scale supply of regulated drug products for domestic and international markets.
Core Responsibilities
- Prepare injectable formulation trials using calibrated balances, mixers, glassware, and controlled environment workstations.
- Develop batch manufacturing records and laboratory notebooks documenting formulation composition, quantities, and step sequences.
- Operate sterilization equipment such as autoclaves and filtration assemblies for parenteral dosage forms.
- Conduct stability sample preparation and place samples in validated stability chambers.
- Compile technical data for regulatory dossiers using standard templates and controlled documents.
- Support scale up trials by adjusting formulation parameters on pilot manufacturing equipment.
Skills and Technical Exposure
- Aseptic compounding tools including laminar airflow units and isolator systems.
- Weighing balances, homogenizers, and solution preparation vessels.
- Autoclaves, sterilizing grade filters, and depyrogenation equipment.
- Stability chambers, temperature monitoring devices, and sampling kits.
- Batch manufacturing records, formulation protocols, and regulatory submission files.
Experience Context
- Work is performed within injectable formulation laboratories and pilot manufacturing areas.
- Activities involve laboratory scale and pilot batches prepared for development and validation studies.
- Absence of this role results in stalled injectable development timelines and incomplete regulatory documentation.
How to Apply
Email vishal.sharma@bdrpharma.com
