ICP-OES, ICP-MS Scientist
2 Positions: Sr. Scientist and Scientist
Sr. Scientist ICP-OES & ICP-MS – Must have 5+ yrs ICP and method validation experience
Lead a small group of chemists to conduct routine QC analysis for the presence of Elemental Impurities in Pharmaceutical grade Raw materials and finished products as well as conducting method development and method validation using ICP-OES, ICP-MS, FAA and GFAA. Responsible to write protocols and report according to the ICH and FDA requirements for method development and method validation for ICP-OES and ICP-MS. Advise Research associate or members of project teams in the initiation and execution of laboratory experimentation. Present results of work, interprets data and draw conclusions regarding presented materials. Maintain full working knowledge of principles and theories, applying such knowledge to the direction that supports Company interests.
Scientist ICP-OES & ICP-MS – Must have 2+ yrs ICP-OES & ICP-MS experience
Conduct routine QC analysis for the presence of Elemental Impurities in Pharmaceutical grade Raw materials and finished products. Learn method validation and gain written protocol experience through mentorship of Sr. Scientist after 90 days. Work under supervision of more senior scientists or scientific directors to advance the development of state-of-art techniques to characterize substances. Demonstrates emerging ability in ability in developing methods, techniques and evaluation criteria for obtaining results and interpreting experimental outcomes