1.Have relevant formulation experience for oral and parenteral dosage forms for new compounds to support in vivo pharmacokinetics, toxicokinetics and pharmacology studies.
2.Have experience with HPLC and other analytical instruments.
3.Generate English protocols, data analysis and reports.
4.Effectively interact and communicate within a dynamic team environment.
5.Well-versed in computer software to support test article receipt and formulation procedures.
Requirements:
The ideal candidate should possess a Ph.D. or M.S. in pharmaceutical chemistry or analytical chemistry with 2-10 years of experience. Experience with formulation preparation, pharmaceutical analysis, analytical method development and validation for small molecules are highly desirable. A candidate is expected to have a good understanding about GLP regulations. Knowledge of pharmacokinetics and drug metabolism in drug research and development are desirable. Demonstrated ability to work independently and in a team environment, and excellent written and verbal communication and good computer skills are required.
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