Manager, Technology Regulatory Compliance

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 Quality Job Sub Function Quality & Compliance Audit Job Category Professional All Job Posting Locations Palm Beach Gardens, FL Raynham, MA West Chester, PA Job Description 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. Learn more at Johnson & Johnson announced plans to separate our Orthopedics 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 Manager, Technology Regulatory Compliance. This is a hybrid role available within United States. While specific states and cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. 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 is required. Advanced degree in a scientific, regulatory, or technical field is preferred. Experience and Skills 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 is required. This position may require domestic and/or international travel. Certifications: Quality or Regulatory certifications are preferred. 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, internal employees contact AskGS to be directed to your accommodation resource. Required Skills Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Compliance Frameworks, Compliance Management, Compliance Policies, Compliance Risk, Critical Thinking, Process Improvements, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Compliance, Risk Management, Technical Credibility, Third-Party Auditing Preferred Skills Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Compliance Frameworks, Compliance Management, Compliance Policies, Compliance Risk, Critical Thinking, Process Improvements, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Compliance, Risk Management, Technical Credibility, Third-Party Auditing Anticipated Base Pay Range $102,000.00 - $177,100.00 Additional Description For Pay Transparency Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). Benefits Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: #J-18808-Ljbffr Johnson & Johnson MedTech