Company Introduction
Gepach International operates regulated pharmaceutical development facilities focused on formulation trials, stability work, and technical documentation.
Core Responsibilities
- Prepare formulation trial samples using balances, mixers, and laboratory-scale processing equipment.
- Document formulation compositions and trial observations in development reports.
- Conduct stability sample preparation and labeling as per approved protocols.
- Maintain laboratory notebooks and formulation development files for each product.
- Support scale-up documentation using pilot batch data and observation sheets.
Skills & Technical Exposure
- Laboratory balances, mixers, and granulation equipment.
- Formulation development reports and protocol documents.
- Stability chamber monitoring records.
- Pharmaceutical excipient compatibility testing methods.
- Regulatory submission support documents.
Experience Context
- Works within formulation development laboratories handling multiple trial batches.
- Supports pilot-scale batches prior to commercial manufacturing.
- Absence of this role delays product development and regulatory documentation timelines.
How to Apply
Interested candidates may send their updated resume to hr@gepach.com