Global UDI PMO Leader: Regulatory & Quality Impact

Johnson & Johnson MedTech; Warsaw (IN); On-site; USD 122,000 - 213,000; Full time

Benefits offered by this job

Vacation 120 hours

Sick leave

Holiday pay

Parental leave

Job summary

Johnson & Johnson MedTech is seeking a Sr Manager, UDI PMO to lead strategic planning and governance for the Global Unique Device Identifier program. You will partner with Quality, Regulatory, IT, and Supply Chain to ensure global regulatory compliance and data integrity.

The role offers high visibility and cross-functional impact across DePuy Synthes portfolios. The position requires 8–10 years in regulated industries, Leadership of complex programs, and experience with ERP and regulatory

Qualifications

• Bachelor’s degree in Engineering, Information Systems, Life Sciences, Quality, or related field is required.

Responsibilities

• Lead the UDI Program Management Office with governance, roadmaps, milestones and metrics.

Skills

Leadership

Global PMO

UDI regulations

Regulatory compliance

ERP integration

Cross-functional collaboration

Education

Bachelor’s degree in Engineering/IS/Life Sciences/Quality

Master’s degree (MS, MBA) preferred

Tools

ERP systems

Regulatory submission systems

Job description

Johnson & Johnson MedTech is seeking a Sr Manager, UDI PMO to lead strategic planning and governance for the Global Unique Device Identifier program. You will partner with Quality, Regulatory, IT, and Supply Chain to ensure global regulatory compliance and data integrity.

The role offers high visibility and cross-functional impact across DePuy Synthes portfolios. The position requires 8–10 years in regulated industries, Leadership of complex programs, and experience with ERP and regulatory