Regulatory Affairs Manager, Special Projects (Acquisition & Divestitures) - MedTech

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Affairs

Job Category:
Professional

All Job Posting Locations:
Atlanta, Georgia, United States, Boston, Massachusetts, United States of America, Charlotte, North Carolina, United States, Cincinnati, Ohio, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, New Brunswick, New Jersey, United States of America, New York, New York, United States, Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Job Description:

We are searching for the best talent for a Regulatory Affairs Manager, Special Projects (Acquisition & Divestitures).

The preferred location for this role is Raritan, NJ however Remote work options may be considered on a case-by-case basis and if approved by the Company.

Purpose: The Regulatory Affairs Manager, Special Projects Acquisitions & Divestitures is responsible for leading regulatory strategies, due diligence and execution support for corporate transactions involving the acquisition, licensing, or divestiture of assets, products or businesses.

This role ensures regulatory compliance and alignment with applicable global health authority requirements throughout the transaction lifecycle.

The selected candidate will ensure the RA A&D Team engages in conversations with global Regulatory Affairs members in the Franchises and Regions to define the path to market for the associated transactions, as required.

You will be responsible for:


* Advice J&J Business Development and other functions on regulatory requirements to enable the successful transfer of assets to or from J&J.


* Develop and execute regulatory strategies and plans for divestitures or acquisition projects.


* Leads Global Regulatory Teams for Medical Device divestitures, and accountable for the overall end-to-end strategy and execution, interfaces with buyers to ensure smooth, compliant and timely transitions of assets.


* Supports negotiations and regulatory clauses in asset purchase, license agreements and/or internal quality plans.


* Represents Global Regulatory Affairs on A&D Project Core Teams, providing strategic considerations for acceleration opportunities and identifying risks an...