Responsibilities
Support oral solid dosage formulation and pharmaceutical process development, including R&D batch preparation, GMP pilot plant activities, and sourcing laboratory supplies. Characterize APIs, develop and test formulations and manufacturing processes, conduct stability studies, prepare prototypes for animal pharmacokinetic studies, and write technical reports.
Requirements
The role requires a B.Sc. in Pharmaceutical Sciences, a master’s degree in Drug Development, or equivalent relevant work experience. It calls for practical capability in pharmaceutical formulation development, API characterization, physical testing, and GMP pilot plant support.
