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Formulation Scientist of Product Development

Job in Lancaster, Lancaster County, South Carolina, 29721, USA
Listing for: Nutramax Laboratories
Full Time position
Listed on 2026-03-04
Job specializations:
  • Research/Development
    Research Scientist
  • Manufacturing / Production
    Food Production
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law).

The hours for this position are Monday - Friday 8:30am - 5:00pm.

Summary of the Position

The Formulation Scientist will provide new product development, product reformulation and process improvement support to a wide range of growth/quality/cost savings projects from ideation through commercialization under direction of the Formulations/Tech Transfer Director. Additionally, this position will work with operations, quality, business teams, and other functional partners; acting as product and process development/improvement support on cross-functional new product development and quality improvement/cost savings teams.

Roles and Responsibilities
  • Capable of formulating moderately complex new products for soft chews, powders, tablets, capsules, pellets, and liquids.
  • Perform bench trials, physical evaluations, and collect data to support new product development.
  • Cooperate with PD staff in preparation/execution of pilot batches and product scale up batches and gather data to support in-process parameters and finished product specifications.
  • Able to direct product development technicians in data collection and processing.
  • Assist in developing new formulations for early-stage development and clinical batches.
  • Work with new equipment/develop studies with equipment that could improve soft chew manufacturing process and/or formulation.
  • Prepare and approve Master Batch Records, Change Control Requests for all scale up or production batches.
  • Follow applicable cGMP processes.
  • Compile and provide summaries of stability data.
  • Provide Technical support to Manufacturing and Operations teams, monitor initial production batches for new and reformulated products.
  • Provide training to manufacturing associates on new processes and process modifications/improvements.
  • Continue education by attending expos and conferences and applying knowledge gained
  • Communicate effectively with other departments within the organization and function within a team environment
  • Regular attendance is required
  • Perform other assigned duties as may be required in meeting company objectives
Qualifications
  • Experience working with soft chew (or similar) dosage forms
  • Excellent interpersonal, communication, and organizational skills
  • Basic ability to define problems, collect data, establish facts, draw valid conclusions, and offer solutions.
Education and Experience
  • BS/BA in chemistry, food science, life sciences, engineering, or a related discipline, or equivalent experience.
  • Must have >5 years of hands‑on experience in product development of food, dietary supplements or related products, including dough, confectionery, or pet treats (animal feed/animal health a plus).
  • Experience in a cGMP environment with understanding of cGMP principles and requirements.
  • Experience working as part of a cross‑functional team.
  • Knowledge of animal feed regulations a plus
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