We seek a highly motivated individual to lead and execute formulation development activities for parenteral dosage forms while maintaining the highest ethical and technical standards. The successful candidate will act as the resident subject matter expert to educate, influence, and implement clinical phase appropriate formulation development strategies. The candidate will be expected to independently execute and document laboratory experimentation, prepare summaries / technical reports, and communicate findings to peers and senior management. The candidate is expected to be familiar with the technical transfer process and regularly interface with contract organizations to support development and manufacturing of drug products. The ideal candidate keeps abreast of key product development technologies, regulatory initiatives, and contract manufacturing landscape.
Preferred Education and Experience: