R&D Formulation Scientist

Job Description

The R&D Formulation Scientist position is responsible for assisting in the design, development, and optimization of dietary supplement products, including capsules, and tablets. This role requires a foundation in formulation science, a strong understanding of chemistry and analytical techniques, and a critical thinking mindset. The ideal candidate will be hands-on, self-driven, and eager to contribute to both the technical and operational success of the R&D function.

In addition to supporting daily lab operations, this position plays a critical role in ensuring product quality through the application of Quality by Design (QbD) principles, process analysis, and data-driven decision-making. The R&D Scientist 1collaborates with cross-functional teams to improve product performance, troubleshoot manufacturing issues, and make evidence-based recommendations to enhance formulations and production efficiency.

Job Duties & Responsibilities:

Formulation Development and Design:

Independently or collaboratively apply scientific methodology to design, modify, and optimize formulas for dietary supplements in various dosage forms. Conduct experimental trials to assess performance, stability, and manufacturability.

Critical Thinking and Innovation:

Apply analytical reasoning and root cause analysis to identify formulation issues and proactively recommend improvements to formulations, equipment, or processes.

Chemistry and Analytical Testing:

Perform laboratory tests and interpret results related to raw material and blend properties, including particle size distribution, moisture content, pH, and density. Use chemistry knowledge to support ingredient compatibility and stability assessments.

Manufacturing Process Support:

Partner with Production and Operations teams to monitor performance of formulations at pilot and commercial scale. Troubleshoot formulation challenges in real time and suggest process or mechanical adjustments to optimize throughput and quality.

Data Collection and Statistical Analysis:

Document process variables and performance data for all trials. Maintain and analyze R&D trackers and technical reports. Use findings to provide updates and insights to the business.

Quality by Design (QbD) & Compliance:

Integrate QbD principles into product development and support continuous improvement. Ensure work adheres to cGMP and company quality standards, SOPs, and regulatory requirements.

Equipment and Laboratory Management:

Prepare test batches, clean and maintain laboratory equipment, and assist with the evaluation or recommendation of new lab or production tools to improve efficiency.

Standard Operating Procedures (SOPs):

Assist in drafting and revising SOPs related to R&D and manufacturing activities to ensure process consistency and knowledge retention.

Continuous Learning and Development:

Stay informed on emerging trends, techniques, and regulatory changes in dietary supplement formulation. Participate in training, cross-functional projects, and scientific discussions to support career growth

Job Requirements:

Schedule requirements: Due to the collaborative and hands-on nature of this role, the scientist is expected to be available during core hours (8:00 AM – 5:00 PM) to interface with production, quality, and R&D teams. Flexibility on these hours or additional hours may be required to support time-sensitive projects or trial coordination.

Minimum Education: Bachelor’s degree in Chemistry, Pharma/Nutra Sciences, Food Science, Biology, or a related scientific discipline.

Experience: 0-2 years in an R&D, QA/QC, or manufacturing role in the dietary supplement, nutraceutical, or food industry.

Skills:

Foundational knowledge of formulation principles and ingredient functionalities.

Understanding of chemical interactions, solubility, and stability.

Familiarity with laboratory practices, data analysis, and scientific documentation.

Strong critical thinking and problem-solving abilities.

Ability to manage tasks independently while collaborating in cross-functional teams.

Proficiency in Microsoft Office (Excel, Word, Powerpoint)

Excellent written and verbal communication skills.

High attention to detail, organization, and time management.

Adaptability and eagerness to learn in a fast-paced, regulated environment.

Experience working under cGMP in a nutraceutical or pharmaceutical environment. (Preferred)

Exposure to dietary supplement regulations (Preferred)

Familiarity with equipment such as tablet presses, encapsulators, and blenders. (Preferred)

Ability to meet deadlines and manage a variety of tasks and priorities.

Full-time