Manager, Regulatory Affairs - Vision

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:
Irvine, California, United States of America, Milpitas, California, United States of America

Job Description:

About Vision

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.

Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.

Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

Your unique talents will help patients on their journey to wellness.

Learn more at https://www.jnj.com/medtech

We are searching for the best talent for a Manager, Regulatory Affairs.  The preferred location for this role is Irvine, CA however candidates within a commutable distance of Milpitas, CA will also be considered.  This role will work a Flex/Hybrid schedule with 3 days per week on-site.  There is NO remote option and relocation assistance is not provided.

Purpose: The Manager, Regulatory Affairs, is a mid-level professional responsible for managing day-to-day regulatory activities, including preparing and submitting registration dossiers and maintaining license compliance.

They provide tactical regulatory support for product lifecycle activities, coordinate with cross-functional teams, and ensure adherence to global regulatory standards.

This role involves direct supervision of projects and contributing to strategic planning, while fostering strong relationships with regulatory bodies to support successful product approvals and lifecycle management.

This role may include management of teams.

You will be responsible for:


* Manages day-to-day regulatory activities including dossier preparation and submission.


* Coordinates with internal teams and external vendors to ensure timely regulatory filings.


* Supports maintenance and renewal of product licenses and registrations.


* Tracks and monitors updates in global regulations impacting assigned products.


* Review...