Job Title: R&D Formulation & Compliance SpecialistOverview
Enova Science is a leading contract manufacturer in the premium supplement and nutrient industry. We are seeking a meticulous, scientifically driven R&D Formulation & Compliance Specialist to join our Product Development team.
In this role, you will sit at the intersection of science, innovation, and regulatory compliance. You will be responsible for translating client concepts into viable, high-quality supplement formulations, conducting deep dive ingredient research, and ensuring all Supplement Facts labels strictly adhere to FDA guidelines. The ideal candidate possesses a strong scientific background, incredible attention to detail, and a passion for the nutraceutical industry.
Key Responsibilities
- Supplement Formulation: Develop, optimize, and scale custom supplement formulations (powders, capsules, tablets, etc.) based on client requests, manufacturing capabilities, and cost targets.
- Label Review & Compliance: Audit, draft, and finalize Supplement Facts panels and ingredient statements to ensure 100% compliance with FDA regulations and labeling laws.
- Ingredient Research & Sourcing: Conduct rigorous research on raw materials, botanicals, vitamins, and minerals to verify efficacy, safety, allergen profiles, and synergy within formulations.
- Technical Documentation: Create and maintain Master Manufacturing Formulas, product specifications, allergen statements, and cross-functional technical data sheets.
- Cross-Functional Collaboration: Partner closely with the Sales/Quotation teams to provide technical insights for client RFQs, and work with Production to troubleshoot pilot batches and scale-up challenges.
Requirements & Qualifications
- Education: Bachelor’s degree in Food Science, Nutrition, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Experience: 2+ years of hands-on experience in R&D, formulation, or regulatory compliance specifically within the dietary supplement, nutraceutical, or food manufacturing industry.
- Regulatory Expertise: Deep understanding of FDA 21 CFR Part 111 (cGMP for Dietary Supplements) and FDA labeling requirements.
- Analytical Skills: Strong research capability to evaluate raw material specifications, Certificates of Analysis (CoAs), and clinical studies.
- Attention to Detail: Absolute precision when calculating active vs. input ingredient overages, serving sizes, and daily values (% DV).
What We Offer
- Competitive salary based on technical experience and qualifications.
- A modern R&D environment within a rapidly growing contract manufacturing facility.
- Health, dental, and vision benefits, along with paid time off.
Pay: $26.00 - $30.00 per hour
Benefits:
- Health insurance
- Paid time off
Education:
Experience:
- Supplement R&D: 2 years (Preferred)
- Supplement Fact Complience: 2 years (Preferred)
Work Location: In person
