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New · posted Oct 14

Johnson & Johnson · Medical Devices

Sr. Source Regulatory Compliance Specialist

  • Palm Beach Gardens, FL +3 more
  • Hybrid
  • Full-time
  • Senior & Principal
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EmploymentFull-time
Deadline

Closes Oct 21, 2026 · 8 days left

The role

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.

DePuy Synthes is recruiting for a Sr. Source Regulatory Compliance Specialist, located in Palm Beach Gardens FL, Raynham MA, Warsaw, IN or West Chester PA.

Job Overview

The Manager, Technology Regulatory Compliance, is responsible for leading compliance activities related to technical and regulatory requirements across the organization in support of product and non-products systems. This role ensures that technical processes, documentation, and system implementations align with applicable regulatory standards, quality system requirements, and internal policies. The position plays a critical role in managing compliance risk, conducting audits and assessments, supporting audit inspection readiness, and enabling compliant execution of technical initiatives by partnering closely with Quality, Regulatory Affairs, Engineering, and IT teams.

What you need

Education

·       Bachelor’s degree in Regulatory Affairs, Quality, Engineering, Life Sciences, Information Systems, or related discipline (required).

·       Advanced degree in a scientific, regulatory, or technical field (preferred).

Required:

·       Typically, 6-8 years of progressive experience in Regulatory Compliance, Quality Systems, Engineering, or related roles within a regulated industry.

·       Strong working knowledge of regulatory and technical requirements impacting quality systems and processes.

·       Experience supporting audits, inspections, and compliance assessments.

·       Ability to manage complex technical compliance topics across cross‑functional stakeholder groups.

Preferred:

·       Experience in medical devices, healthcare, or other highly regulated industries.

·       Familiarity with EMEA regulatory and technical compliance frameworks.

·       Experience working in a global or matrixed organization.

·       Exposure to regulatory inspections involving technical or system compliance.

·       Quality or Regulatory certifications (e.g., RAC, ASQ).

·       Strong analytical, risk‑management, and problem‑solving skills.

·       Effective written and verbal communication skills.

Other:

·       Language: English required; additional European languages preferred.

·       Travel: Moderate regional travel across EMEA.

·       Certifications: Quality or Regulatory certifications preferred but not required.

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 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.

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.

Preferred Skillsnice to have

Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Communication, Compliance Management, Compliance Policies, Compliance Risk, Controls Compliance, Critical Thinking, Problem Solving, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)

What you'll do

·       Lead and manage technology regulatory compliance activities, ensuring adherence to regulatory and quality system requirements.

·       Provide compliance oversight for technology processes, systems, and documentation supporting regulated activities.

·       Interpret regulatory and technology standards and translate them into actionable compliance requirements.

·       Partner with Quality, Regulatory Affairs, Engineering, and IT teams to support compliant systems and process implementation.

·       Conduct internal audits, external audits, and support health authority inspections in support of product and non-product technology regulatory compliance.

·       Monitor compliance risks, trends, and performance metrics; drive corrective and preventive actions.

·       Ensure consistent application of global and regional compliance policies, procedures, and controls.

·       Drive continuous improvement initiatives to strengthen technical compliance, governance, and effectiveness.

Where you'll work

Palm Beach Gardens, FL +3 moreHybridOpen in Maps (opens in a new tab)

Also posted for: West Chester, PA · Warsaw, IN · Raynham, MA

More jobs in Palm Beach Gardens, FL +3 more

Working conditions

Job Function

Quality

Job Sub Function

Quality & Compliance Audit

Job Category

Professional

All Job Posting Locations

Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word

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.

Job intelligence

The context around this role

Live data · October 14, 2026

Salary intelligence

How the pay compares

Senior & Principal roles in the US8 roles publishing pay

Middle half $127,125 to $169,500, median $150,500
Annual base pay
Annual base payLowMedianHigh
All US$127,125$150,500$169,500

Comparisons: the base pay employers published on open Compliance roles at the same level on Regulatory Jobs, October 14, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Compliance

The general path across 31 open Compliance roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Associate, Quality Records · Co-Op, Compliance and Data QC

    $84K median6 open
  2. This role

    Senior & Principal

    Often: Principal Quality Compliance and Policy Leader · Principal Quality Compliance Specialist, CVRM

    $151K median9 open
  3. Next step

    Manager

    Often: AQR Quality Program, Manager · Commercial Quality Controlled Substance Manager

    $161K median6 open
  4. Later

    Director

    Often: Associate Director, CMC Quality Compliance and Inspection Readiness · Director CMC Quality Compliance

    $220K median8 open
  5. Later

    VP & Executive

    Often: Head of Quality Compliance

Skills DNA

What this role leans on

How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 15 linesLab testing and methods: 2 linesDocumentation and SOPs: 4 linesRegulatory submissions: 1 lineQuality systems and risk: 5 linesCollaboration and leadership: 6 linesGMPLab testingDocumentationSubmissionsQuality systemsTeamwork
  • GMP and compliance15
  • Collaboration and leadership6
  • Quality systems and risk5
  • Documentation and SOPs4
  • Lab testing and methods2
  • Regulatory submissions1

Company hiring pulse

Johnson & Johnson on Regulatory Jobs

36
Open roles
36
Distinct roles
15
Locations

By discipline

  • Quality24 67%
  • Regulatory7 19%
  • Compliance & Safety5 14%

By level

  • Senior & Principal11 31%
  • Manager9 25%
  • Director8 22%
See all 36 Johnson & Johnson roles

More roles at Johnson & Johnson

All 36 Johnson & Johnson roles

Similar Compliance roles elsewhere

Sr. Source Regulatory Compliance Specialist at Johnson & Johnson

Applications close October 21.

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