About this role
Kenvue is currently recruiting for a:
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®, TYLENOL®, 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:
助理法规经理Location:
Asia Pacific, China, Shanghai, ShanghaiWork Location:
HybridWhat you will do
- 100% Sufficient regulatory and registration strategy in place and delivered for NPD and renovation projects to help support NTS/GP improvements , compliance and business continuity.
- Having accurate regulatory assessment and making sure right regulatory action being taken for product whole life cycle, making sure no non-compliance risk during post market supervision.
- Proactively finishing internal compliance tasks to meet internal process and requirements, maintain RA information in internal system
- Ensures compliance with regulatory agency regulations and interpretations.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.
About Kenvue
Consumer health company spun off from Johnson & Johnson, maker of Tylenol, Listerine, and Band-Aid brands. Based in Skillman, NJ.
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