Research and Development Manager; Dietary Supplements Manassas, VA
Listed on 2026-06-26
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Manufacturing / Production
Pharmaceutical Manufacturing, Regulatory Compliance Specialist
We are seeking a high-caliber R&D Manager to lead the formulation and lifecycle management of our diverse product portfolio. With over 60 active SKUs spanning high-performance powders and encapsulated supplements, you will be the bridge between innovative "bench-top" concepts and scalable, profitable manufacturing.
You will be responsible for new formulas testing, optimizing existing formulas for cost and flowability, and ensuring 100% compliance with FDA 21 CFR Part 111 and SQF Edition 9 standards.
Key Responsibilities- Portfolio Mastery:
Manage and optimize a catalog of 60+ SKUs. - Formulation & Innovation:
Lead the "Bench-to-Bottle" process for new powders and capsules. Develop robust masking strategies for bitter botanicals and minerals. - Scale-Up Leadership:
Oversee the transition from R&D lab batches to full-scale production (Blending & Encapsulation). Troubleshoot floor issues such as clumping, capping, or flowability. - Technical Documentation:
Manage document changes and updates, including Master Manufacturing Records (MMR). - Cross-Functional Synergy:
Collaborate daily with the Plant Manager on production efficiency and the Supply Chain Specialist to qualify alternative raw material vendors, as well as existing remote R&D team. - Fix any product related issues on the production floor (powder density, flowability, color, blending, etc.).
- Lead R&D team on site, manage all projects related to new or existing products.
- Education:
B.S. in Food Science, Chemistry, or Pharmaceutical Science (M.S. or Ph.D. strongly preferred). - Experience:
3-5 years of direct R&D experience in the Dietary Supplement or Pharmaceutical industry. At least 2 years in a leadership or project management capacity. - Technical Expertise:
Proven experience formulating complex powder blends and two-piece capsules. - Deep understanding of excipient functionality (glidants, lubricants, fillers).
- Regulatory Fluency:
Expert knowledge of FDA 21 CFR Part 111 and SQF requirements.
- Full-time, on-site role.
- 4 weeks of paid vacation per year.
- 7 annual paid holidays.
- Comprehensive health insurance.
- 401(k) plan eligibility.
We are a growing dietary supplement manufacturer specializing in high-quality powder formulations. Our focus is on combining science, manufacturing excellence, and great consumer experience — including taste. As we expand, we’re looking for driven, hands‑on experts who want to make a real impact and help shape the future of our product portfolio.
Why Join Us?This is an opportunity to play a key role in building standout products in a fast-growing company. You’ll have real ownership, work on challenging formulations, and directly influence the quality and success of products in the market.
Start Date:
ASAP
Location:
Ability to work on-site in our Northern Virginia, Manassas facility to support the production floor.
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