Labeling Compliance Specialist

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:
Supply Chain Engineering

Job Sub Function:
Manufacturing Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Danvers, Massachusetts, United States of America

Job Description:

About Cardiovascular

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 the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.

You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

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

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

This is role will be available in Danvers, MA in the United States.

Remote work may be eligible.

While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.

We invite candidates from any location to apply.

We are searching for the best talent for a Labeling Compliance Specialist.

Purpose: Johnson & Johnson is seeking an experienced and detail-oriented professional to join our team as a Labeling Compliance Specialist.

This individual will ensure compliance with all relevant regulations and standards related to product labeling, while contributing to the development, assessment, and lifecycle management of labeling strategies.

They will collaborate with cross-functional teams including Regulatory, Clinical, Quality, Design, and Lifecycle to evaluate changes for new product launches and revisions.

With a strong background in project management and a solid understanding of regulatory standards for medical devices, they will oversee labeling initiatives to ensure our portfolio remains compliant.

This role offers an exciting opportunity to influence product compliance on a global scale.

Principal Duties and Responsibilities:


* Ensure personal and company compliance with all federal, state, local, and company regulations, policies, and procedures related to product labeling and instructions for use (IFU).


* Complete the Label Assessment, including redlining artwork, file creation, and translation management.


* Serve as the point pers...