ADL OfficerSrOfficerExecutive

We areseeking a highly skilled person to join the team in thepharmaceutical industry. The ideal candidate will be responsiblefor method development and validation as well as routine andstability analysis utilizing a variety of analytical techniquesincluding HighPerformance Liquid Chromatography (HPLC) GasChromatography (GC) Dissolution testing and Karl Fischertitration.

• Developand validate analytical methods for the quantitative analysis ofpharmaceutical compounds using HPLC GC Dissolution and KFtechniques.
  
• Performroutine analysis of pharmaceutical samples according to establishedprotocols andprocedures.
  
• Conductstability studies to assess the stability of pharmaceuticalformulations overtime.
  
• Troubleshootand optimize analytical methods to ensure accuracy precision andreliability ofresults.
  
• Maintainaccurate records of all analyses method development and validationactivities in compliance with regulatoryguidelines.
  
• Collaboratewith crossfunctional teams including R&D Quality Controland Regulatory Affairs to support product development andregulatorysubmissions.
  
• Staycurrent with developments in analytical techniques instrumentationand regulatory requirements in the pharmaceuticalindustry.