The Research Scientist I is responsible for the design, development, optimization, and scale-up of dietary supplement products from concept through commercial manufacturing within a CDMO / white-label environment. This role requires strong formulation fundamentals across multiple dosage forms, with the ability to balance customer requirements, consumer centricity, cost targets, regulatory requirements, and manufacturing feasibility. Experience with gummies and flavored dosage forms is a strong plus. The successful candidate will demonstrate versatility across dosage forms and the ability to rapidly learn and adapt to new technologies and formats. Provides technical leadership on moderately complex development programs, supports customer-facing innovation, and plays a key role in ensuring formulations are robust, scalable, and commercially viable. The candidate must be comfortable working cross-functionally with R&D, Quality, Regulatory, Supply Chain, and Manufacturing in a fast-paced, customer-driven CDMO environment Formulate dietary supplement products in response to customer requests ranging from highly defined specifications to open-ended innovation briefs Conduct bench-scale trials, physical evaluations, and data collection to support formulation decisions Support and participate in sensory evaluations and tasting panels for flavored dosage forms Develop and maintain costed formulations, including raw material, processing, and packaging assumptions Prepare and maintain formulation specifications, technical documentation, and development reports Collaborate with Quality and Regulatory teams to proactively address compliance, labeling, and claims considerations Provide ongoing technical support to internal stakeholders and external customers throughout development, scale-up, and commercialization Continuously improve formulation approaches, platforms, and best practices based on customer needs, market trends, and manufacturing learnings Prepare, review, and approve Master Batch Records (MBRs), Master Change Requests (MCRs), and other formulation-related documentation Provide hands-on technical support during manufacturing trials and initial commercial production runs Execute responsibilities with minimal supervision while managing multiple projects Ownership & Accountability – Takes responsibility for outcomes from concept through commercialization Collaboration & Influence – Works effectively across R&D, Quality, Regulatory, and Operations without formal authority Resilience in Ambiguity – Thrives in fast-paced, changing environments typical of CDMO operations Perform other duties as assigned
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
501-1,000 employees