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Regulatory Affairs Specialist

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Job ID:
2607045601W
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Kenvue is currently recruiting for a:

Regulatory Affairs Specialist

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:

法规事务经理

Location:

Asia Pacific, China, Shanghai, Shanghai

Work Location:

Fully Onsite

What you will do

75% – Project RA Execution Support for LCM Activities

  • Support regulatory activities for product life cycle management (LCM) projects under supervision.

  • Assist in compiling, formatting and organizing regulatory submission dossiers in accordance with regulations and internal requirements.

  • Support preparation of routine variation submissions and documentation updates.

  • Assist in drafting responses to standard or routine Health Authority (HA) questions under guidance.

15% – Regulatory Intelligence & Documentation Support

  • Support tracking of updates to local regulatory regulations, guidelines and technical notices.

  • Assist in summarizing regulatory changes and supporting impact assessments for ongoing projects.

  • Support maintenance of regulatory documentation, databases and internal records.

5% – External Interaction Support

  • Support maintenance of regulatory documentation, databases and internal records.

5% – Other RA Activities

  • Support maintenance of regulatory documentation, databases and internal records.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.