The individual will assist with the review of technical documentations (i.e. manufacturing executed batch records, process development reports, manufacturing reports, analytical reports, etc.)
The individual may also be asked to independently conduct synthesis and process development activities for preclinical and clinical candidates. This includes laboratory experimentation for compound preparation, synthetic route scouting, process development/optimization and process trouble-shooting. Additional responsibilities include support for off-site synthesis and interaction with scale-up/manufacturing contractors. The individual is expected to effectively document research and to conduct work in a safe manner in accordance with company and departmental guidelines.
BS in science with a minimum of two years experience in the pharmaceutical/process development field. Excellent interpersonal skills with strong oral and written communication skills. Must be proficient in Microsoft Office. Understanding of organic chemistry, process chemistry, GLP and GMP is highly desired.