Senior Scientist- Self Care

Senior Scientist- Self Care What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. Role Reports To RES. MANAGER ORAL DRUG DELIVERY TECH. Location North America, United States, New Jersey, Summit Work Location Fully Onsite What You Will Do Self‑Care is a core strength for Kenvue with ambitious goals to grow the portfolio through product innovation and scientific leadership in priority markets. To support this growth, we need experienced technical talent who can deliver strong science, lead complex programs, and help develop the next generation of scientists. We are seeking a highly skilled Senior Scientist to join our Self‑Care Future of Kenvue Innovation team. This role requires a strategic thinker with strong formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self‑care solutions. The successful candidate will manage multiple projects, solve complex technical challenges, and help shape the strategic direction of our R&D efforts. This role requires a high degree of autonomy and collaboration in a fast‑paced, regulated environment. Key Responsibilities Lead the design, formulation, and development of innovative self‑care products, with a focus on solid, semi‑solid and liquid dose forms. Design and execute strategies to overcome technical challenges in product formulation and manufacturing processes. Collaborate with product development and technical teams to ensure seamless technology transfer. Ensure compliance with FDA regulations and GxP standards throughout the development process. Stay current with regulatory guidelines and industry standards to ensure compliance and best practices. Utilize fundamental project management skills to track progress, mitigate risks, and deliver results. Communicate complex scientific and technical information effectively to both technical and non‑technical stakeholders. Participate in initiatives such as patent reviews, scientific forums, and safety leadership programs. Shape the scientific strategic planning and decision‑making processes related to product development and portfolio management, aligning R&D activities with broader business objectives. Demonstrate business acumen by understanding the impact of R&D activities on the company's overall goals. Required Qualifications Bachelor’s Degree with 5+ years or Master’s degree with 3+ years of relevant experience. Degree must be in Materials Science, Biomedical Engineering, Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related discipline. Experience in early‑stage product development within the consumer health care or pharmaceutical industry . Proficiency in formulation development, process optimization, and/or analytical techniques. Experience with QbD (Quality by Design) principles is required. Experience in typical unit operations such as granulation, roller compaction, drying, milling, blending, compression/encapsulation, film coating, and spray drying etc. Knowledge and experience with regulatory requirements including ICH, FDA, compendia (e.g. USP, JP, EP, etc.) is highly preferred. Proven track record of managing complex projects, with strong organizational and leadership skills. Excellent project management skills, including timeline management, and team coordination. Flexibility in schedule to support global teams and willingness to travel up to 25% domestically and internationally. Desired Qualifications Proven experience in solid and liquid dose formulation and manufacturing (tablets, capsules, soft chews, gummies). Proven experience in formulation of liquid and semi‑solids for topical, oral and/or nasal applications. Experience in supporting FDA filings such as NDA, PAS, ANDA, 510K, RFD, etc. Demonstrated leadership by influence and ability to mentor and develop team members. Foundational understanding of FDA regulations and guidelines for pharmaceutical product development. What’s In It For You Annual base salary for new hires in this position ranges: $105,400.00 - $148,800.00 Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation. #J-18808-Ljbffr Kenvue