We are seeking a highly skilled person to join the team in the pharmaceutical industry. The ideal candidate will be responsible for method development and validation as well as routine and stability analysis utilizing a variety of analytical techniques including HighPerformance Liquid Chromatography (HPLC) Gas Chromatography (GC) Dissolution testing and Karl Fischer titration.
Responsibilities:
- Develop and validate analytical methods for the quantitative analysis of pharmaceutical compounds using HPLC GC Dissolution and KF techniques.
- Perform routine analysis of pharmaceutical samples according to established protocols and procedures.
- Conduct stability studies to assess the stability of pharmaceutical formulations over time.
- Troubleshoot and optimize analytical methods to ensure accuracy precision and reliability of results.
- Maintain accurate records of all analyses method development and validation activities in compliance with regulatory guidelines.
- Collaborate with crossfunctional teams including R&D Quality Control and Regulatory Affairs to support product development and regulatory submissions.
- Stay current with developments in analytical techniques instrumentation and regulatory requirements in the pharmaceutical industry.
Knowledge of Liquid Chromatography (HPLC), Gas Chromatography (GC), Dissolution testing, and Karl Fischer titration.