# Senior Regulatory Affairs Program Lead (Wound Closure & Healing) - MedTech Surgery at Johnson & Johnson

Johnson & Johnson is hiring a Senior Regulatory Affairs Program Lead (Wound Closure & Healing) - MedTech Surgery for a remote role open to applicants in United States. It pays $109k-$175k a year and Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/3fdc9c72-d0c9-456d-9a0e-f09da0891d94?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Remote (Raritan, New Jersey, 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: Remote (Raritan, New Jersey, United States of America)
- Salary: $109k-$175k
- Posted: October 14, 2026
- Apply: https://jobsbylevel.com/go/3fdc9c72-d0c9-456d-9a0e-f09da0891d94?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: Raritan, New Jersey, United States of America, Remote (US) Job Description: About Surgery 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 surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. 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 Senior Regulatory Affairs Program Lead to support our Wound Closure and Healing group. Preference will be given to candidates located within a commutable distance of Raritan, NJ however remote work options will be considered on a case by case basis and if approved by the company . Purpose : The Senior RA Program Lead has end to end responsibility for the life cycle maintenance and new product development launches within the Wound Closure and Healing portfolio. The Senior Regulatory Affairs Program Lead provides independent regulatory guidance to product development teams in strategic planning, pre-marketing, and related submissions to support optimal timelines for new/modified global product launches. Under little to no supervision, the individual leads the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers to support new, modified and currently marketed medical devices. He/she guides conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials. The Senior RA Program Lead helps to define data and information needed for regulatory approvals in conjunction with cross-functional product development teams. The role assists in the identification and development of best practices for Regulatory Affairs processes. You will be responsible for : · Represent Regulatory Affairs on cross functional teams and serve as a regulatory SME on projects, including partnering with other functions to define and obtain data to assist with regulatory submissions. · Provide input and guidance during New Product Development and Lifecycle Change Management projects, including regulatory strategy and supporting evidence including clinical data. · Prepare expert responses to regulatory agencies' questions and other correspondence. · Prepare and submits regulatory information required to obtain timely US and EU market access, including preparation, writing and filing of FDA submissions (e.g., Q-submissions, IDEs, De Novo, 510(k)s) and EU MDR submissions. · Lead the submission of licenses and authorizations for the maintenance of existing products,

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/senior-regulatory-affairs-program-lead-wound-closure-healing-medtech-surgery-at-johnson-johnson-100999

Source: https://jobsbylevel.com/jobs/senior-regulatory-affairs-program-lead-wound-closure-healing-medtech-surgery-at-johnson-johnson-100999

## Cite this page

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