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Johnson & Johnson

Manager, Global UDI

Johnson & Johnson

Manager, Global UDI at DePuy Synthes ensuring UDI compliance across orthopedic portfolio. Leading initiatives for regulatory compliance and data integrity in global markets.

Posted 6/8/2026full-timeRaynham • Massachusetts, Pennsylvania • 🇺🇸 United StatesMid-LevelSenior💰 $117,000 - $234,000 per yearWebsite

Tech Stack

Tools & technologies
ERP

About the role

Key responsibilities & impact
  • Lead and govern the global UDI program, ensuring compliance with FDA, EU MDR, and other applicable international UDI regulations
  • Own UDI-related quality processes, procedures, and controls, ensuring alignment with standards
  • Partner with IT and digital teams to ensure UDI system design, validation, data integrity, and ongoing system compliance
  • Provide quality oversight for UDI data management, including master data accuracy, change control, and issue remediation
  • 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 processes
  • Drive continuous improvement initiatives to enhance UDI governance, efficiency, and compliance sustainability
  • Provide coaching and leadership to team members and stakeholders to strengthen UDI and quality capabilities across the organization

Requirements

What you’ll need
  • Bachelor’s degree in Engineering, Life Sciences, Information Systems, or a related field
  • 6–8 years of relevant 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)
  • Strong knowledge 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 regulatory inspections
  • Strong analytical, problem-solving, and risk-based decision-making skills
  • Excellent written and verbal communication skills
  • Experience working with enterprise systems supporting UDI and product data (e.g., ERP, PLM, labeling systems) preferred
  • Prior people-leadership or matrix leadership experience preferred
  • Experience within orthopedics or complex medical device portfolios preferred
  • Familiarity with global supply chain and labeling processes preferred
  • Change management or continuous improvement experience in regulated environments preferred
  • English (additional languages a plus)

Benefits

Comp & perks
  • 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 period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year

ATS Keywords

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Hard Skills & Tools
UDI regulationsquality systemsdata governancecomputerized system validationregulatory compliancequality assurancechange managementcontinuous improvementrisk-based decision-makinganalytical skills
Soft Skills
leadershipcross-functional collaborationproblem-solvingcommunication skillscoachingstakeholder engagementmatrix leadershipteam managementorganizational skillsadaptability