Kenvueは現在、a:
私たちがしていること
Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.
Who We Are
私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.
Role reports to:
Director, Regulatory Affairs, Self Care Lead場所:
Europe/Middle East/Africa, United Kingdom, England, High Wycombe勤務地:
ハイブリッドあなたがすること
Kenvue is currently recruiting for a:
Senior CMC Specialist (Self Care)
This position is based at our High Wycombe office (hybrid working policy). 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.
Who We Are
At Kenvue, we realise 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.
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 across the Global and Regional Regulatory Self Care team.
Responsible for meeting compliance requirements within team such as SOP trainings, audits etc.
Partner with other critical functions to execute plans to address crises and other sensitive issues.
Serves as a CMC lead for the deployment of CMC regulatory technical content, submissions and compliance activities for Self Care medicinal products supporting.
Provides and supports technical and operational global CMC regulatory direction and documentation for assigned projects/products covering post approval activities.
Lead the preparation of CMC information for submission to global regulatory agencies, generates and deploys CMC technical content, assesses risks and develops contingency/mitigation plans.
Acts as the global/regional CMC representative within cross-functional project teams, involving the interpretation of regulations and guidelines and the assessment of global implications for technical CMC decisions.
Primary accountable for assigned CMC programs, managing daily delivery of regulatory and technical activities, including post-approval changes ,and ongoing compliance of commercial products in the portfolio.
May represent CMC during interactions with internal and external partners either directly or in conjunction with Global Regulatory Affairs Teams.
Resolve issues and manage regulatory risks within project teams. Investigates opportunities for regulatory improvement / promote the use of novel approaches within project team to resolve issues and problems.
Experience Required
Relevant Bachelor's Degree or higher
Sound knowledge in the regulatory requirements of post approval changes for global markets including ICH guidance
Sufficient level of knowledge in handling post approval changes of Solid Oral, nasal sprays and other Dosage forms in addition to manufacturing and regulatory data requirements for managing Global post approval submissions.
Knowledge in retrieving information from company’s and regulatory agency databases.
Good level of knowledge on general standards, processes and policies around manufacturing medicinal products.
Proficiency in English
What we are looking for
Excellent communication skills, with the ability to articulate and express concepts clearly and persuasively both verbally and in writing, particularly when simplifying complex regulatory or technical issues.
Strong interpersonal skills; able to build effective personal networks internally and externally.
Highly collaborative with a strong sense of ownership, willing to be held accountable and be rewarded for delivering results.
Strong organizational and time management skills with an ability to work under pressure.
Demonstrable commercial focus and business acumen which will enable him/her to thrive in a fast-paced, dynamic, Results-driven environment.
In-depth knowledge of the business, organizational goals, Regulatory Affairs function, and cross functional business partners to make informed business decisions and create and execute business strategies. Ability to represent RA function on cross-functional teams and governance forums.
Able to work effectively in a multi-cultural, highly matrixed organization
What’s in it for you
Competitive Benefit Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups
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 identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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