NOTE: This role does NOT offer sponsorship for work authorization. External applicants must be eligible to work in the US. Candidates must have a minimum of 2-3 years pharmaceutical industry experience to be considered.
This is a 1-year Contract role. In this role, the Process Associate Scientist I/II will involve developing and optimizing pharmaceutical manufacturing processes, ensuring product quality and consistency, and complying with regulatory requirements on commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts pilot scale manufacturing activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.
Essential Duties and Responsibilities
Qualification Requirements
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