The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities.
Requirements
- GMP compliance in formulation and process development
- Assisting 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
- Lead efforts in solving formulation and process problems
- Directly support with writing batch records, SOPs, IQ/OQ/PQ documents, development/technical reports, and CMC sections for regulatory submissions as directed
- Ensure that all work is accurate, precise, properly documented and, when appropriate, performed within GMP guidelines
- Eight or more years of experience in pharmaceutical development with focus on solids formulation required
Benefits
- 152 hours of PTO
- 8 paid holidays
- 401k Matching
- Retirement Plan