Dietary Supplement Formulator (Liquid Supplements & Multi-Form Factor Products)

GENCANNA ACQUISITION CORPWinchester, KY
1dOnsite

About The Position

The Dietary Supplement Formulator is a senior, hands-on technical role responsible for the formulation, optimization, and commercialization of dietary supplement products, with primary emphasis on liquid supplements and complex vitamin-fortified systems. The role supports products delivered across multiple form factors, including liquids, tinctures, gummies, and capsules, within an FDA-registered, cGMP manufacturing environment. The position owns formulation development end to end, from concept and prototyping through costing, scale-up, and commercial production, working closely with Sales, Manufacturing, Quality, Finance, and Supply Chain. GenLabs.health (GenCanna) is a U.S.-based finished goods manufacturer of dietary supplements and wellness products operating FDA-registered, cGMP-compliant facilities. The company formulates and manufactures liquid supplements, tinctures, gummies, softgels, capsules, and topicals for internal brands and external partners.

Requirements

  • Bachelor’s degree in a relevant scientific discipline
  • Minimum five (5) years of dietary supplement formulation experience
  • Strong experience with liquid and vitamin-fortified systems
  • Proven commercial scale-up experience in cGMP environments

Responsibilities

  • Develop and refine liquid dietary supplement formulations, including complex vitamin and mineral blends
  • Design formulations platformed across liquids, tinctures, gummies, softgels, and capsules
  • Manage solubility, stability, ingredient interaction, and flavor challenges
  • Formulate CBD-containing products where applicable, as one ingredient among many
  • Support Sales with rapid, credible, and commercially competitive formulation concepts
  • Source and evaluate ingredients; assess feasibility and suppliers
  • Build formulation-level cost models
  • Own scale-up from bench to commercial production
  • Collaborate with Manufacturing to troubleshoot and improve yields
  • Ensure FDA and cGMP compliance
  • Prepare and maintain technical documentation
  • Partner with Quality on stability and audit readiness

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