# Senior Regulatory Affairs Specialist at Johnson & Johnson

Johnson & Johnson is hiring a Senior Regulatory Affairs Specialist. It pays $109k-$175k a year and Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/49d2716a-6210-41c8-a51b-41102f3bbd9e?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. West Chester, Pennsylvania, United States of America.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 37 out of 100)
- Location: West Chester, Pennsylvania, United States of America
- Salary: $109k-$175k
- Posted: October 21, 2026
- Apply: https://jobsbylevel.com/go/49d2716a-6210-41c8-a51b-41102f3bbd9e?utm_medium=ai-agent

## Description

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 jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Regulatory Affairs Group Job Sub Function: Regulatory Affairs Job Category: Professional All Job Posting Locations: Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America, Zuchwil, Switzerland Job Description: About Orthopaedics 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 Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes We are searching for the best talent for Senior Regulatory Affairs Specialist in West Chester, PA , Raynham, MA. JOB SUMMARY Coordinates, compiles, and submits medical devices applications and investigational medical device applications to the regulatory bodies. DUTIES & RESPONSIBILITIES In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: · Leverages scientific and technical understanding of regulated products within scope of responsibility (mainly NPD/NPI) to provide regulatory input to product lifecycle management and evaluate regulatory impact on products. · Compile, prepare, review, and submit regulatory submission to regulatory authorities. · Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities for division orthopedic devices. · Interface with Product Development to obtain necessary information for regulatory submissions. · Review / approve Change Requests / Notices to determine the level of change and consequent submission requirements. · Review/approve product labeling: device labels, brochures, technique guides, bulletins, updates, etc. · Prepare registration documents, medical device listings, and

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/senior-regulatory-affairs-specialist-at-johnson-johnson-52c46d

Source: https://jobsbylevel.com/jobs/senior-regulatory-affairs-specialist-at-johnson-johnson-52c46d

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