Senior Associate, Global Category Medical Affairs - Vitamins, Minerals & Supplements
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
As an R&D Category Senior Associate, you will drive innovation across Reckitt’s Global VMS (Vitamins, Minerals & Supplements) portfolio. You will apply scientific expertise and strategic insight to support the development, evaluation, and optimization of new and existing products. Working cross‑functionally with Marketing, Innovation, Product Development, Clinical, and Regulatory, you will help shape medical evidence strategies, guide scientific assessments, and ensure our products meet rigorous healthcare and consumer standards.
Your responsibilities
- Support the development and execution of medical and evidence strategies for VMS innovation and product development.
- Conduct literature reviews and evaluate efficacy/safety data to guide feasibility assessments and substantiation.
- Provide scientific input into innovation concepts, ingredient evaluations, and new product ideas.
- Collaborate closely with cross‑functional partners to ensure medical accuracy and alignment across programs.
- Serve as a scientific contributor for claims development, evidence packages, and regulatory documentation.
- Review and support development of medical‑marketing materials and scientific communication assets.
- Monitor scientific publications, ingredient developments, and competitor activity to inform strategic direction.
- Support medical governance requirements, including documentation, compliance, and training material preparation.
The experience we're looking for
- Master’s or PhD in a Life Science; specialization in Human Nutrition preferred.
- 2+ years of experience in consumer health, nutrition, OTC, pharmaceutical, medical device, or similar industries (internships included for junior profiles).
- Experience evaluating scientific evidence, clinical literature, or product substantiation.
- Strong scientific and medical writing skills with the ability to synthesize complex information.
- Familiarity with regulated product environments (e.g., supplements, OTC, medical devices).
- Exposure to cross‑functional collaboration with Marketing, R&D, Commercial, or Regulatory teams.
- Knowledge of evidence generation, healthcare regulations, or KOL engagement is beneficial.
- Ability to work in a fast‑paced, matrixed environment with sound organizational and prioritization skills.
The skills for success
Medical & Scientific Writing, Scientific Literature Review, Evidence Evaluation, Efficacy & Safety Assessment, Claims Substantiation, Healthcare Regulations, Compliance & Governance, Medical Science Support, Cross-Functional Collaboration, Business Partnership, Commercial Awareness, Stakeholder Management, Relationship Management, Influencing Without Authority, Competitive Intelligence, Ingredient Landscape Monitoring, Innovation Support, Product Lifecycle Support, Task Execution Under Pressure, Objective Setting, Accountability, Adaptability, Consumer Insight, Presentation Skills, Training Content Development.
What we offer
US salary ranges
US pay transparency
Equality

Nearest Major Market: Newark
Nearest Secondary Market: New York City
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Medical Device, Counseling, Nutrition, Medical, Healthcare