Job Responsibilities

- Perform analytical method development and method validation for pharmaceutical formulations.
- Execute analytical method transfers and troubleshooting activities.
- Conduct analysis using HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution, and other analytical instruments.
- Prepare analytical protocols, reports, specifications, Standard Test Procedures (STPs), and Standard Operating Procedures (SOPs).
- Perform stability sample analysis and support product development activities.
- Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines.
- Maintain laboratory documentation in accordance with data integrity requirements.
- Perform calibration, verification, and routine maintenance of analytical instruments.
- Investigate Out of Specification (OOS), Out of Trend (OOT), and laboratory deviations.




- Coordinate with cross-functional teams including Formulation Development, QA, QC, and Regulatory Affairs.
- Ensure proper housekeeping and adherence to laboratory safety practices.

Key Skills

- Hands-on experience with HPLC, GC, UV, FTIR, Dissolution, and other analytical instruments.
- Robust knowledge of analytical method development and validation.
- Understanding of ICH guidelines, cGMP, GLP, and data integrity.
- Good documentation and report-writing skills.
- Strong analytical, problem-solving, and communication skills.
- Ability to work independently and as part of a team.

📌 Adl Officer (Gujarat)
🏢 BioMatrix Healthcare
📍 Gujarat