• Job title US Regulatory Leader, Heart Recovery
• Function Regulatory Affairs Group
• Sub function Regulatory Affairs
• Category Senior Director, Regulatory Affairs (P10)
• Location Danvers / United States of America
• Date posted Feb 24 2026
• Requisition number R-060268
• Work pattern Hybrid Work

This job posting is anticipated to close on Mar 04 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

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.

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Johnson & Johnson Med Tech is recruiting for a Sr, Director, US Regulatory Affairs, Heart Recovery located in Danvers, Massachusetts!

About MedTech

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

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

About Cardiovascular

Are you passionate about improving and growing the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops 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.

We are seeking an experienced, strategic, and externally recognized regulatory thought-leader to drive complex regulatory projects, involving cross-functional teams, in support of the organization's business priorities. Knowledge in the field of cardiovascular medical devices with a proven record in regulatory strategy, policy and pre- and post-market submissions, particularly in the US is required. This individual will lead a team of regulatory professionals (FTE and contractor) who are accountable for all product registrations with a focus on the US FDA, in collaboration with cross-functional teams, including R&D, Clinical, Quality, Supply Chain and Global Strategic Marketing, to enable timely development and execution throughout the total product life cycle of innovative cardiovascular devices. The role will act as the primary regulatory lead for interactions with FDA, and will establish industry-leading regulatory approaches that support business objectives and patient access to innovative cardiovascular products. This role has significant market & business level influence and responsibility and is considered a leader and an FDA authority resource within Heart Recovery. This Sr. Director will be actively called upon for shaping and advocating for emerging regulations and policies. This leader will lead a team that will support regulatory activities including NPD, Lifecycle Management / Base Business, and cross-business unit regulatory activities.

The right leader will support US market approvals and ensure regulatory compliance for a ground-breaking heart recovery business that will accelerate patient access to life-saving cardiac therapies.

Key Responsibilities:

• Lead development of regulatory strategies through total product lifecycle management for assigned cardiovascular products
• Serve as the primary Regulatory contact for the FDA
• Provide subject matter expertise for preparation, review, and submission of regulatory filings including 510k, IDEs, PMAs, HDEs, post-market actions and safety communications, ensuring high-quality regulatory documentation and submissions
• Provide regulatory expertise during product development, including development of clinical trial strategies ensuring compliance with relevant clinical and device regulations and standards
• Identify and communicate to senior leadership regulatory risks and opportunities across programs and define mitigation strategies that balance patient safety, compliance, and business timelines
• Leads, mentors, develops regulatory team members and builds capability across functions
• Participate in governance, risk assessments, and go/no‑go decisions for critical product development goals

Leadership Competencies

• Executive Presence: Communicates complex regulatory rationale clearly and confidently to senior leaders and partners.
• Critical Thinking: Builds regulatory strategies that align with product lifecycle and global business goals.
• Influencing & Partner Management: Drives alignment across cross-functional and regional teams without direct authority.
• Critical Leadership: Makes timely, risk‑balanced decisions in uncertain regulatory environments and guides teams through complexity.

Qualifications

Education:

• Bachelor’s degree in life sciences, biomedical engineering, engineering, pharmacy, or related field required
• Advanced degree (MS, PhD, PharmD) strongly preferred

Experience and Skills:

Required:

• Minimum of 15 years of regulatory affairs experience in the medical device with demonstrated experience leading regulatory strategies across major geographies (U.S., EU, APAC).
• At least 5 years of increasing leadership experience, including leading complex teams or program-level regulatory activities.
• Consistent track record preparing and submitting high‑complexity regulatory filings (e.g., IDEs, PMAs) and interacting directly with the FDA.
• Excellent written and oral communication skills with demonstrated ability to present in senior level environments and to external partners.

Preferred:

• Deep experience in cardiovascular or implantable device development and regulatory strategy.
• Previous experience at the FDA.
• Experience with combination products, software as a medical device (SaMD), or digital health components.
• Experience with breakthrough device/designation pathways or accelerated regulatory pathways.
• Proven understanding of global regulatory requirements, submission and clinical trial regulations/standards.

Other:

• English Proficiency required
• 20% Travel Required, including international.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.]

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource

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