Development Scientist II
About The Position
The Development Scientist II is a primary client contact for pharmaceutical development and clinical manufacturing projects. The role supports supervision, process development, clinical trial batch manufacturing, packaging, and documentation. The scientist is responsible for formulation and process development across several ongoing projects, including project management and customer contact. This position is 100% on-site at Catalent’s Greenville, North Carolina site, which provides end-to-end solutions for oral solid dosage forms, including formulation development, analytical services, commercial manufacturing, and packaging.
Requirements
- Bachelor’s degree in Pharmacy, Chemistry, Biology, or a related field and at least eight years of experience in pharmaceutical development focused on solid formulations; or a master’s degree in Pharmacy, Pharmaceutics, Industry Pharmacy, or a related field and at least six years of pharmaceutical development experience; or a Ph.D. in Pharmacy, Pharmaceutics, Industry Pharmacy, or a related field and at least four years of pharmaceutical development experience.
- Some exposure to hazardous chemicals and other active chemical ingredients.
- Ability to handle and manipulate objects using hands and arms.
- Ability to occasionally lift items weighing more than 50 pounds.
- Ability to wear a respirator, contingent on completing a medical evaluation with satisfactory results.
Responsibilities
- Ensure GMP compliance in formulation and process development.
- Assist with planning and operating within a budget for the pharmaceutical area.
- Work directly with customers and potential customers to agree on development approaches and scope of work.
- Assist the manufacturing group with batch manufacture and packaging/labeling, including setup and cleaning.
- Lead efforts to solve formulation and process problems.
- Support the writing of batch records, SOPs, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions, as directed.
- Ensure work is accurate, precise, properly documented, and performed within GMP guidelines when appropriate.
- Perform other duties as assigned.
Benefits
- 152 hours of PTO
- 8 paid holidays
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What This Job Offers
Job Type
Full-time
Career Level
Senior
