Senior Manager CMC, Regional Lifecycle Management

Come work at the forefront of science – and help the brands you grew up with grow and evolve into the next generation.

Job Description – Senior Manager CMC, Regional Lifecycle Management (2507034022W)

Location: London

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. Science is our passion; care is our talent. Our global team of 22,000 diverse and brilliant people is passionate about insights, innovation, and committed to delivering the best products to our customers. Being a Kenvuer means having the power to impact the lives of millions every day. We put people first, care fiercely, earn trust with science, and solve with courage. Join us in shaping our future—and yours.

Role Overview:

The Senior Manager CMC & Regional Lifecycle Management leads a team responsible for the post-approval lifecycle management of the regional Self Care portfolio across the EMEA region.

Responsibilities:

1. Develop and execute global CMC and post-approval regulatory strategies with a focus on compliance.
2. Identify documentation requirements and address content, quality, and timeline issues for submissions, supporting the delivery of approved technical documents.
3. Oversee authoring/review of high-quality CMC/core labelling documentation, ensuring regulatory compliance and adherence to timelines.
4. Implement risk management strategies for product lifecycle maintenance, proactively communicating risks and strategies to project teams and stakeholders.
5. Lead, prepare, and communicate CMC & Labelling Risk Management Assessments, contingency plans, and lessons learned.
6. Manage Health Authority interactions and negotiations, including briefing preparations and risk mitigation.
7. Create an environment of operational excellence through regulatory expertise, managing and developing team members, and collaborating across functions.
8. Develop strong partnerships with R&D, Franchise, Operations, and local regulatory teams.
9. Represent Regulatory Affairs in Self Care Franchise, functional, and business leadership teams.

Qualifications:

• Bachelor’s Degree or higher in a relevant field.
• Experience across regulatory classifications including Drugs, Dietary Supplements, and Medical Devices.
• Knowledge of regulatory frameworks and product lifecycle solutions.
• Strong understanding of post-approval change requirements, including ICH guidelines.
• Experience with post-approval changes for solid oral, nasal sprays, and other dosage forms.
• Understanding of regulatory, medical, safety, and quality requirements in relevant markets.
• Leadership and coaching skills with experience in people development.
• Proficiency in English.

What’s in it for you:

Learning & Development Opportunities. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration 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.

Primary Location:

Europe/Middle East/Africa – United Kingdom – England – High Wycombe

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