Primary responsibility of the position is to support all Research and Development activities and  further enhance small molecule bioanalysis capabilities.  In this role, the qualified candidate will work as part of a multi-disciplinary team to design and implement traditional and innovative R&D programs.  This work combines all aspects of pre-clinical development and validation, study design, data analysis report and summary presentations.

Responsibilities include developing and validating multidimensional analytical and bioanalytical methods to characterize and quantify small molecules.

Qualifications:

• Ph.D. degree
• 8-10 years of experience in the pharmaceutical / biotechnology / CRO industry related to drug development including method development and validation in GLP/GMP regulated environment. 
• Experience with ESI-MS, MALDI TOF MS, HPLC, CE, CE-MS, affinity separation, electro-analytical  methods, UV and FTIR spectroscopy and LIF detection.   In-depth knowledge of physico-chemical analysis in solution and at interfaces is desired.  
• Extensive experience in sample preparation techniques, including dialysis, solid phase extraction and semi preparative chromatography is required.    
• Experience in analysis of complex biological samples, hyphenated, and multidimensional analysis, and in high throughput method development is essential.   
• Prior supervisory experience is an advantage.