Senior CMC Specialist (Self Care)

Description

Kenvue is currently recruiting for:

Senior CMC Specialist (Self Care)

This position reports to Director Regulatory Affairs Self Care and is based at High Wycombe.

Kenvue have announced a planned move of offices to Reading, Berkshire in Q1 of 2026.

Please note that this role will move locations along with this office move.

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®, 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.

For more information, click here .

Role reports to: Director Regulatory Affairs Self Care

Location: High Wycombe

What you will do

The Senior CMC Specialist is responsible for the Life Cycle Management (LCM) activities of assigned products and/or projects providing regulatory assessments and deploying regulatory technical content across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product development teams within the Self Care franchise.


* Acts as the global/regional (as relevant) CMC representative within cross-functional project teams.

Accountable for assigned projects and activities, completing work within assigned product portfolio.

Develops resolution proposals for regulatory CMC issues with the stakeholders.



* Reviews proposed CMC changes for completeness and accuracy, interpret CMC regulatory requirements, deploys technical content, assess risks and develops contingency proposals.

Use technical and scientific knowledge to conduct the analysis of CMC submission documentation.



* Oversees the authoring and review of CMC documentation, coordination and management of global submissions, including the assessment and management of commercial license status, maintenance of product compliance and management of change control.



* Represents the Regulatory Affairs function as appropriate within the Self Care Franchise.



* Provide regulatory support to policy, external engagement, and issue management within the Need State of responsibility and participate in process, simplification & culture-building activities within own team and across enterprise as required.



* Co-responsible for supporting alignment of key processes, ways of working and simplifications a...