What are the responsibilities and job description for the Research And Development Scientist position at Crescent Edge Consulting?
An R&D Scientist with 5 years' experience in product development is need for a leading dietary supplement manufacturing company in Provo, UT. The successful candidate will leverage a strong foundation in scientific principles to develop innovative supplement formulations and optimize manufacturing processes from proof of concept through scale-up, validation, and implementation. This role requires a proactive problem-solver with a passion for excellence and a commitment to continuous improvement in a dynamic, team-oriented environment.
R&D Scientist Responsibilities:
- Design and develop novel supplement formulations tailored to diverse product categories.
- Optimize and characterize formulation processes, ensuring alignment with manufacturing capabilities and product safety standards.
- Proactively monitor, investigate, and resolve issues related to formula stability and product quality.
- Design and execute bench and pilot scale experiments, validating new products for seamless transition to full-scale manufacturing.
- Analyze experimental data, prepare detailed technical reports, and effectively communicate findings to management and cross-functional teams.
- Serve as a reliable technical resource, providing expert support for product characterization and manufacturing operations.
R&D Scientist Requirements:
- Bachelor’s degree in Biology, Chemistry, or a related science; Master of Science (MS) is strongly preferred.
- Minimum of 5 years’ experience in product development with extensive formulation knowledge across a variety of material types (e.g., solids, water-soluble powders, emulsions).
- Proven experience managing product development projects from proof of concept through scale-up and manufacturing transition.
- Strong background in food, beverage, and personal care product components, with a keen understanding of formulation challenges.
- Excellent verbal and written communication skills, with demonstrated experience in preparing technical reports and controlled documents.
- Prior experience working in a GMP/GLP regulated environment, emphasizing quality, safety, and regulatory compliance.
- Ability to manage multiple projects in a fast-paced environment while maintaining a high standard of work and attention to detail.
Benefits:
- Comprehensive benefits (medical, vision, and dental insurance)
- Free products and discount program
- 401K plan w/ employer matching & FSA
Salary : $90,000 - $110,000
