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Sr. Source Regulatory Compliance Specialist

Job in Warsaw, Kosciusko County, Indiana, 46580, USA
Listing for: Johnson & Johnson MedTech
Full Time position
Listed on 2026-08-29
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 110000 - 150000 USD Yearly USD 110000.00 150000.00 YEAR
Job Description & How to Apply Below

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 Med Tech, 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

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

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

Job Description

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.

Key Responsibilities
  • 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.
Qualifications 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 Experience and Skills
  • 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…
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