Regulatory Affairs, Self-Care Manager

Description

Kenvue is currently recruiting for a:

Regulatory Affairs, Self-Care Manager

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:
DIRECTOR REGULATORY AFFAIRS

Location:
North America, United States, New Jersey, Summit

Work Location:
Hybrid

What you will do

The Manager, Regulatory Affairs will have regulatory responsibility for products across needs-states including within the Pain Franchise (which includes key brands such as TYLENOL®, MOTRIN®, and BENGAY®); and for several products in development that include a wide range of Regulatory classifications (NDA/ANDA and Monograph Drugs, Dietary Supplements, Medical Devices and Combination products).

The candidate will be the primary contact with the Food and Drug Administration for NDA/ANDA and Monograph Drug submissions.

Key Responsibilities


* Understand the Regulatory landscape for Consumer products and manage regulatory priorities, projects and activities for marketed products and will support and/or lead regulatory strategy for innovative projects.


* Labeling, digital, promotional review and approval, as well as other project execution and post-market related activities.


* Routine submissions to FDA, which may include preparing meeting requests and meeting background packages to FDA.


* Support and/or lead FDA interactions and ensure that meeting objectives are met and ensure the strong reputation of the Company is maintained.


* Strong leadership representing Regulatory on project teams providing expertise and alternatives to optimize strategy and claims, and/or in optimizing processes and/or systems related to regulatory activities.


* Use knowledge of regulatory landscape, competitive benchmarking, external factors to shape and inform regulatory strategy.


* Demonstrate successful collaboration and partnership across teams and functions within the organization.


* Lead process improvement workstreams.


* Monitor regulatory environment for new industry standards, FDA guidances, regulations, and draft legislation for impact to the business.

Work with industry association(s) to ...