Senior Scientist, Self Care R&D - Johnson & Johnson Consumer Inc.

Senior Scientist, Self-Care Product and Process Development

Location: Initially at Fort Washington, PA with expected transition to new Kenvue World Headquarters in Summit, NJ by end of 2026

Who we are

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. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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. For more information, click here .

Reports To: Associate Director R&D, Self-Care Product and Process Development

Job Type: Full-Time

Travel Requirement: Up to 25% domestic and international

What You Will Do We are seeking a motivated and experienced Senior Scientist to join Self-Care Product and Process Development team. Reporting directly to the Associate Director, this role focuses on supporting the development and optimization of consumer health products, with an emphasis on over-the-counter (OTC) medications and supplements. The Senior Scientist will play a critical role in ensuring product efficacy, safety, and compliance with regulatory standards. The ideal candidate will have a strong background in formulation science, process development, and experience in GxP (e.g. GDP, GMP, GCP) compliance.

Key Responsibilities:

• Lead consumer centric formulation and development of consumer health products, including OTC medications, dietary supplements, and personal care items, ensuring they meet quality and efficacy standards.

• Exercise considerable latitude in determining technical objectives and in selecting techniques and evaluation criteria for obtaining resolution to complex and dynamic problems in consultation with manager.

• Identify and resolve technical challenges in product and process development, utilizing sound scientific principles and experimental data under general guidance.

• Support the optimization of manufacturing processes to enhance efficiency, scalability, and robustness.

• Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project.

• Work closely with cross-functional teams, including R&D, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals.

• Stay up-to-date with the latest scientific advancements and incorporate them into research projects

• Prepare and maintain detailed documentation for product development processes, including experimental protocols, batch records, and technical reports in compliance with Good Documentation Practices (GDP)

What we are looking for Required Qualifications:

• Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Engineering, Biomedical Engineering, Biophysics, or a related field.

• Ph.D. in Pharmaceutical Sciences 0-2yr, M.S. with 3 years of relevant experience, or Bachelor's Degree with 4 years of relevant experience.

• Strong knowledge of formulation science, process development, and foundational understanding of regulatory requirements for OTC medications and dietary supplements.

• Proficiency in analytical techniques and methods used in product development and quality control.

• Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely.

• Ability to work collaboratively within a multidisciplinary team and across various functions.

• Strong analytical and problem-solving skills.

Desired Qualifications

• Experience in product and process development within the consumer health industry.

• Experience in solid dose formulation and manufacturing (tablets, capsules, soft chews, gummies).

• Experience in formulation of liquid and semi-solids for ingestion, topical, and/or nasal application.

• Demonstrated ability to manage multiple projects and work effectively in a fast-paced environment.

• Proficiency in project management skills, including timeline management, budget oversight, and team coordination.

What's in it for you

• Competitive Benefit Package*

• Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!

• Learning & Development Opportunities

• Employee Resource Groups

• 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 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.

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