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R D Formulation Specialist (Dietary Supplements) 1955 West Grove Parkway, Pleasant Grove, UT 84062 $18 - $35 an hour - Full-time Apply with

Indeed Pay:

$18.00 to $35.00 per hour, based on experience About the Role PAG Pharmatech America LLC (www.pagpharmatechusa.com) provides custom formulation and US-based contract manufacturing for dietary supplement and nutraceutical brands. We are looking for an R D Formulation Specialist to develop supplement formulas and make samples for our clients and in-house product lines. The role covers formula development and review for conventional dosage forms (hard capsules, tablets, powders, stick packs and gummies) as well as two growing lines: oral pouches and soft chews. Hands-on sampling covers powders, tablets, hard capsules, oral pouches and soft chews. You will turn a client's concept or target label into a formula that works on the production line, meets FDA dietary supplement rules, and can be quoted accurately, working closely with sales, supply chain and production from first inquiry through approved sample and scale-up.

Key Responsibilities Formula development:

Turn client concepts, target labels and benchmark products into complete formulas, including actives, excipients, flavors, sweeteners and processing aids. Convert label claim amounts into raw material input using each ingredient's actual assay or potency, with appropriate overages to meet label claim through shelf life. Check every formula against unit capacity (capsule size, tablet weight, scoop or stick fill, pouch fill, chew weight) before costing. Support each recommendation with a clear basis such as clinical literature, regulatory limits or comparable market products. Review formulas for FDA dietary supplement compliance (DSHEA, NDI status, ingredient safety limits). Prepare formula sheets with ingredient specs and target cost so sales and supply chain can quote quickly.

Conventional dosage forms:

Develop and review formulas for hard capsules, tablets, powders, stick packs and gummies. Gummy work covers formulation and formula review only, with no sampling. Solve technical problems such as flowability, compression, blend uniformity, dissolution, solubility, taste masking and color stability.

Oral pouches:

Develop nicotine-free functional oral pouch formulas (for example energy, focus, fresh breath and oral care) in the dry pouch format. Control particle size, bulk density, moisture, flowability and fill weight consistency. Work on flavor, sweetness, cooling, release rate and mouthfeel. Support machine trials and adjust formulas when a blend does not run well.

Soft chews:

Develop soft chew formulas for human and pet supplement applications. Balance active loading against texture, palatability, water activity and shelf stability. Select binders, humectants, fats and flavors suited to the process, and support scale-up on high-speed automated forming equipment.

Sampling and testing:

Make bench and pilot samples of powders, tablets, hard capsules, oral pouches and soft chews, and coordinate samples made by partner factories when needed. Keep sampling fast and organized so clients receive samples on schedule. Run or arrange basic testing such as appearance, weight variation, moisture, water activity, disintegration, taste panels and stability checks. Write clear sample notes and revise formulas based on client feedback.

Documentation and support:

Maintain formula records, batch records, raw material specifications and change history. Prepare product specifications, Supplement Facts panel drafts and ingredient statements. Work with supply chain on raw material sourcing, alternative ingredients and COA review. Answer technical questions from sales and clients. Follow cGMP practices (21 CFR Part 111) in all lab and sampling work. Required Qualifications Bachelor's degree or higher. A degree in Food Science, Nutrition, Chemistry, Pharmaceutical Science, Biochemistry or a related field, or work experience in the dietary supplement industry. Either background is acceptable. Solid knowledge of common supplement ingredients, including vitamins, minerals, botanical extracts, amino acids, probiotics and their typical assay and potency. Working knowledge of FDA dietary supplement regulations, cGMP (21 CFR Part 111) and Supplement Facts labeling.

Comfortable with formula math:

potency conversion, overages, batch scaling and cost per unit. Able to manage several sample projects at once and hit deadlines. Clear written and spoken English for technical documents and client communication. Authorized to work in the United States. Preferred Qualifications Master's degree in a related field. Hands-on formulation experience with oral pouches, soft chews, tablets, hard capsules or powders. Experience with pet supplement soft chews and familiarity with AAFCO and NASC requirements. Experience transferring formulas from bench to commercial production with a contract manufacturer. Familiarity with branded and patented ingredients and their licensing or claim requirements. Experience with stability study design and shelf-life setting. Working Conditions On-site, Monday to Friday, 9:00 AM to 5:00 PM, with time split between our Pleasant Grove office and our Spanish Fork production facility. The work involves standing for long periods, handling powders and raw materials, and wearing PPE in production areas. Lifting up to 50 lb may be required. To apply, send your resume and a short summary of products you have formulated. Mobile (WhatsApp/WeChat): +1 385 521 6376

Email:

xd@pagpharmatechamerica.com PAG America is an equal opportunity employer. Employment is at-will.

Pay:

$18.00 - $35.00 per hour

Benefits:

Paid time off

Work Location:

In person