ADL OfficerSrOfficerExecutive

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.

• 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.