EU MDR Regulatory Project Manager – MedTech

Johnson & Johnson Co.; Ledston; Sur place; GBP 75 000 - 100 000; Plein temps

Résumé du poste

Johnson & Johnson is seeking a Principal Project Manager in the UK to lead regulatory submissions under MDR for DePuy Synthes Orthopedics. You will manage timelines, coordinate with Notified Bodies, and align cross-functional teams to achieve franchise goals.

The role requires strong project management skills, regulatory knowledge in medical devices, and the ability to drive complex submissions with stakeholders across business units.

Qualifications

• Bachelor’s degree in project management, regulatory affairs, life sciences, engineering, or related discipline.
• Master’s degree preferred.

Responsabilités

• Coordinates EU Notified Body submissions and project tracking for new product introductions and changes.
• Develops and maintains detailed project plans, timelines, and status reports for stakeholders and leadership.
• Identify risks and issues, mitigate, and escalate as needed.
• Represent DePuy Synthes with EU Notified Body in regulatory filings and meetings.
• Maintain MDR certificate data and documentation.

Connaissances

Project management

Regulatory affairs

Cross-functional leadership

Scheduling

Communication

MS Office

Formation

Bachelor’s degree in project management, regulatory affairs, life sciences, engineering, or related discipline

Master’s degree

Outils

MS Office

Description du poste

Johnson & Johnson is seeking a Principal Project Manager in the UK to lead regulatory submissions under MDR for DePuy Synthes Orthopedics. You will manage timelines, coordinate with Notified Bodies, and align cross-functional teams to achieve franchise goals.

The role requires strong project management skills, regulatory knowledge in medical devices, and the ability to drive complex submissions with stakeholders across business units.