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Research and Development Manager (Dietary Supplements)

  • On-site
    • Virginia, United States
  • Manufacturing

Job description

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.

Job requirements

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, such 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

Requirements & Qualifications

  • 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.

Working Hours & Benefits

  • Full-time, on-site role

  • 4 weeks of paid vacation per year

  • 7 annual paid holidays

  • Comprehensive health insurance

  • 401(k) plan eligibility

About the Company

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.

Details

On-site
  • Manassas, Virginia, United States
Manufacturing

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