DevelopmentScientistI

**Development Scientist I** **Position Summary:** * **Work Schedule:** Monday-Friday, 8:00am-5:00pm EST * This position is 100% on-site at the Greenville site. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Development Scientist I will serve as the primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development Scientist I is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. **The Role** * Independently design and execute experiments. * Solve formulation and process problems. * Author SOP’s, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions. * Maintain competency and training for relevant processes and equipment. * Ensure that all work is accurate, precise, properly documented, within GMP requirements. * Organize multiple project responsibilities to ensure tasks are appropriately prioritized and executed on time. * Design, coordinate, and execute development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises. * Ongoing communication with clients, internal support groups, resources, vendors and staff. * All other duties as assigned. **The Candidate** * Bachelor’s degree in pharmaceutical science, chemistry, engineering, or related science with at least three years of industrial pharmaceutical experience. * Master’s degree in pharmaceuti