At a Glance
- Tasks: Lead regulatory CMC strategy for new product development and manage lifecycle activities.
- Company: Join Kenvue, a global leader in everyday care with iconic brands.
- Benefits: Enjoy a hybrid work model, competitive salary, and a supportive culture.
- Other info: Collaborative environment with opportunities for professional growth and innovation.
- Why this job: Make a real impact in healthcare by ensuring product compliance and quality.
- Qualifications: Bachelor's degree and 10+ years in regulatory affairs or pharmaceutical development.
The predicted salary is between 63000 - 77000 £ per year.
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. 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. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you!
Acts as regulatory CMC lead in new product development projects with responsibility for regulatory CMC strategy development and deployment.
Leads a team of regulatory affairs CMC product owners with responsibility for Module 3/CMC maintenance ensuring the success of life cycle management activities and roll-out of existing products.
Develop strong partnerships with Regulatory Affairs partners, R&D, Marketing and Supply Chain.
Represents the Regulatory Affairs CMC function as appropriate in various regulatory and cross-functional teams and technical fora.
Creates an environment of operational excellence through regulatory expertise, management of CMC product owners and collaboration with cross-functional teams.
- Relevant Bachelor's Degree or higher
- ~10+ years experience from regulatory affairs and/or pharmaceutical product development
- ~ Expertise across regulatory classifications including medicinal products and medical devices as it relates to pharmaceutical CMC regulatory affairs
- ~ Knowledge of regulatory frameworks globally as it concerns pharmaceutical product development and CMC requirements
- ~ Strong project and people management skills
- ~ Proficiency in English
This process is important for us to ensure the quality of our recruitment process.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.
Regulatory Affairs Manager - Remote in Sonning Common employer: Kenvue
At Kenvue, we foster a vibrant work culture where every voice is valued and innovation thrives. As a Product Lifecycle Manager in Reading, you'll enjoy a hybrid work environment, competitive benefits, and ample opportunities for professional growth while contributing to the success of iconic brands that impact millions. Join us to be part of a team that prioritises care, collaboration, and continuous improvement in the supply chain landscape.
