Johnson & Johnson

Global UDI

Johnson & Johnson$79K — $142K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Computer Science, Information Systems, Life Sciences, or related discipline.
  • 4-8 years of experience in Quality Assurance, Quality Systems, or regulatory roles within medical devices or pharmaceuticals.
  • Experience with validated systems in regulated environments.
  • Knowledge of global UDI regulations (e.g., FDA, EU MDR) and quality system requirements.
  • Ability to analyze quality data and drive continuous improvement.

Responsibilities

  • Oversee global UDI technology platforms to ensure regulatory compliance and data integrity.
  • Develop and maintain UDI-related quality processes and controls throughout the product lifecycle.
  • Collaborate with IT and stakeholders to validate and maintain UDI systems in compliance with regulations.
  • Review and approve UDI documentation, including validation deliverables and procedural updates.
  • Monitor UDI data accuracy and compliance with internal and external regulatory databases.
  • Assist with audits, inspections, and interactions with health authorities regarding UDI.
  • Identify quality risks and improvement opportunities in UDI processes and digital solutions.

Benefits

  • Opportunity to influence enterprise-level quality and digital transformation initiatives.
  • High visibility and global impact within the organization.
  • Cross-functional collaboration with diverse teams.
  • Training opportunities on UDI requirements and quality standards.
  • Potential for career advancement in a reputable medical device company.
Full Job Description
Job Function:
Project/Program Management Group

Job Sub Function:
Project/Program Management

Job Category:
Professional

All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, 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(n) Global UDI located in Raynham, Massachusetts

The Global UDI role plays a critical part in ensuring DePuy Synthes' global compliance with Unique Device Identification (UDI) regulatory requirements through robust quality oversight of enabling technologies, systems, and processes. This position partners cross-functionally with Regulatory Affairs, IT, Supply Chain, and Manufacturing to ensure UDI data accuracy, system validation, and sustained compliance across global markets. The role offers high visibility, global impact, and the opportunity to influence enterprise-level quality and digital transformation initiatives supporting patient safety and regulatory excellence.

Key Responsibilities

  • Provide oversight for global UDI technology platforms, data flows, and supporting systems to ensure regulatory compliance and data integrity.


  • Support development, implementation, and maintenance of UDI-related quality processes, procedures, and controls across the product lifecycle.


  • Partner with IT and business stakeholders to ensure UDI systems are validated, maintained, and compliant with applicable quality system regulations.


  • Review and approve UDI-related documentation, including system validation deliverables, change controls, risk assessments, and procedural updates.


  • Monitor and assess UDI data accuracy, completeness, and timeliness across internal systems and external regulatory databases.


  • Support internal and external audits, inspections, and health authority interactions related to UDI and supporting technologies.


  • Identify quality risks, trends, and improvement opportunities related to UDI processes and digital solutions; drive corrective and preventive actions.


  • Provide quality guidance and training to cross-functional partners on UDI requirements, quality standards, and system controls.


Qualifications

Education

  • Required: Bachelor's degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related discipline.


  • Preferred: Advanced degree in Quality, Regulatory, or a technical field.


Experience and Skills

Required:

  • Typically 4-8 years of experience in Quality Assurance, Quality Systems, or Regulatory-adjacent roles within medical devices, pharmaceuticals, or regulated industries.


  • Experience supporting validated systems and technology platforms in a regulated environment.


  • Working knowledge of global UDI regulations (e.g., FDA, EU MDR) and quality system requirements.


  • Experience with change control, risk management, and documentation review within a quality framework.


  • Demonstrated ability to analyze quality data, identify trends, and drive continuous improvement.


Preferred:

  • Experience with UDI databases, labeling systems, or enterprise data management platforms.


  • Familiarity with computer system validation (CSV) and digital quality controls.


  • Experience supporting regulatory inspections or audits related to data integrity or digital systems.


  • Knowledge of Lean, Six Sigma, or continuous improvement methodologies.


  • Experience working in a global or matrixed organization.


  • Strong collaboration skills with the ability to work effectively across global, cross-functional teams.


Other:

  • Language: English proficiency required.


  • Travel: Up to ~10-15%, domestic and occasional international.


  • Certifications: ASQ certifications (e.g., CQA, CQE) or similar quality certifications preferred.


Required Skills:

Preferred Skills:
Agility Jumps, Analytics Insights, Business Alignment, Business Behavior, Collaboration Tools, Communication, Cost-Benefit Analysis (CBA), Data Analysis, Monitoring, Evaluation, and Learning (MEL), Problem Solving, Process Oriented, Project Management Methodology (PMM), Project Management Office (PMO), Project Reporting, Project Support, Statement of Work (SOW), Time Management

The anticipated base pay range for this position is :
79,000.00 - 1,42,000.00 USD Annual

Additional Description for Pay Transparency:

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

Work You’ll Do

At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

Transform Health Care

Leverage Johnson & Johnson’s culture of innovation to transform health care and improve the lives of people around the world. Our collaborative environment encourages leadership and growth, allowing you to pioneer new strategies for health care solutions with a diverse team of experts.

Innovative Work

Engage in groundbreaking work that enhances how care is delivered on a global scale. Johnson & Johnson’s commitment to innovative health solutions results in dynamic career paths filled with opportunities for professional growth and development.

Be Part of a Great Team

Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

Future-Proof Your Career

Johnson & Johnson offers a myriad of job opportunities and employment benefits designed to help you meet your career and personal goals. Our employees enjoy comprehensive benefits, including health insurance, retirement plans, and family-friendly policies that pave the way for a fulfilling career and life balance.

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Whether you’re looking to start your career or take it to the next level, Johnson & Johnson offers positions ranging from internships to leadership roles across various sectors. Enhance your skills through hands-on experience and our extensive networking and mentorship programs.

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Our commitment to leadership and continuous learning is at the core of our employment philosophy. Every position offers chances to lead, learn, and innovate. We provide extensive training programs and development courses that prepare you for the future of health care.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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