Job Function:
Project/Program Management Group
Job Sub Function:
Project/Program Management
Job Category:
People Leader
All Job Posting Locations:
Irvine, California, United States of America, Jacksonville, Florida, United States of America, Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson MedTech is recruiting for a Manager, Global UDI Regulations and Data Strategy located in Raritan, NJ, Irvine, CA and Jacksonville, FL! An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
The Manager, Global UDI Regulations and Data Strategy is a key leadership role within J&J MedTech, responsible for ensuring global compliance, data strategy, and execution of Unique Device Identification (UDI) requirements across the J&J MedTech portfolio. This role partners closely with Regulatory Affairs, IT, Supply Chain, R&D, and Commercial teams to ensure UDI data capabilities, process readiness, and regulatory compliance across global markets.
This position offers the opportunity to lead a globally impactful compliance program that directly supports patient safety, product traceability, and regulatory readiness while shaping scalable, future‑ready UDI processes and systems.
Key Responsibilities- Lead and govern the global UDI program, ensuring compliance with FDA, EU MDR, and other applicable international UDI regulations.
- Drive strategy for functional data use within UDI Health Authority records.
- Own UDI‑related processes, procedures, and controls, ensuring alignment with Technology Quality and quality/regulatory standards.
- Partner with technology and digital teams to ensure capabilities are established and maintained to meet UDI requirements.
- Lead cross‑functional collaboration with Regulatory Affairs, Supply Chain, Manufacturing, R&D, and Commercial teams to ensure end‑to‑end UDI execution.
- Support and participate in regulatory inspections, internal audits, and health authority interactions related to UDI compliance.
- Monitor global regulatory trends and translate new or evolving UDI requirements into scalable business and quality management system processes.
- Drive continuous improvement initiatives to enhance UDI data utilization, efficiency, and compliance sustainability.
- Provide coaching and leadership to team members and stakeholders to strengthen UDI knowledge and capabilities across the organization.
QualificationsEducation
- Required: Bachelor’s degree in Engineering, Life Sciences, Information Systems, or a related field.
- Preferred: Master’s degree in a scientific, technical, or business discipline.
Experience and SkillsRequired:
- 6–8 years of proven experience in Quality Assurance, Regulatory Compliance, or Technology Quality within a regulated industry (medical devices strongly preferred).
- Demonstrated experience with UDI regulations and global regulatory frameworks (e.g., FDA, EU MDR).
- Solid understanding of quality systems, data governance, and computerized system validation.
- Proven ability to lead cross‑functional, global initiatives in a matrixed organization.
- Experience supporting audits and/or regulatory inspections.
- Strong analytical, problem‑solving, and risk‑based decision‑making skills.
- Excellent written and verbal communication skills.
Preferred:- Experience working with enterprise systems supporting UDI and product data (e.g., ERP, PLM, labeling systems).
- Prior people‑leadership or matrix leadership experience.
- Experience within complex medical device portfolios.
- Familiarity with new product introduction, global supply chain, and labeling processes.
- Change management or continuous improvement experience in regulated environments.
Other- Language: English (additional languages a plus).
- Travel: Up to 15%, domestic and international.
- Certifications: ASQ, RAC, or equivalent quality/regulatory certifications preferred.
Required Skills:
Preferred Skills:
Agile Decision Making, Analytics Insights, Business Alignment, Developing Others, Inclusive Leadership, Leadership, Monitoring, Evaluation, and Learning (MEL), Organizational Project Management, Program Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Stakeholder Engagement, Statement of Work (SOW), Team Management
The anticipated base pay range for this position is :
$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)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off 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
Additional information can be found through the link below.
The following link to general company benefits information MUST also be included in the posting: Please use the following language:
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
