Senior Project Manager, MDR Submissions (MedTech)

Johnson & Johnson Co.; Lancashire; On-site; GBP 90,000 - 130,000; Full time

Job summary

Johnson & Johnson is seeking a Principal Project Manager to lead regulatory submissions for Orthopedics under MDR. You will coordinate EU Notified Body interactions, develop project plans, and drive cross-functional execution to support franchise goals.

Join DePuy Synthes to advance safer, compliant medical devices, with exposure to global regulatory strategies and high-impact product approvals.

Qualifications

• Bachelor’s degree in project management, regulatory affairs, life sciences, engineering, or related scientific discipline.
• Master’s degree preferred.
• 5–8 years of project management experience in medical devices or regulated environments.
• Strong planning, scheduling, and organizational skills.
• Excellent communication and stakeholder management abilities.

Responsibilities

• Coordinates submissions to EU Notified Bodies and tracks new product introductions and changes.
• Liaises with business units to ensure proper execution of submissions.
• Develops and maintains detailed project plans, timelines, and status reports.
• Identifies risks and issues and implements mitigation plans.
• Coordinates MDR certificate data and documentation.
• Represents DePuy Synthes with EU Notified Body and regulatory meetings.
• Establishes outlines, summaries, and slides for regulatory filings.
• Interacts with EU regulators to expedite submissions.
• Facilitates relationships with Notified Bodies through regular meetings.
• Works with global Regulatory Affairs to align local and global strategies.

Skills

5–8 years experience in project mgmt

Cross functional projects

Project planning

Scheduling

Organizational skills

MS Office

Education

Bachelor’s degree

Master’s degree

Tools

MS Office

Job description

Johnson & Johnson is seeking a Principal Project Manager to lead regulatory submissions for Orthopedics under MDR. You will coordinate EU Notified Body interactions, develop project plans, and drive cross-functional execution to support franchise goals.

Join DePuy Synthes to advance safer, compliant medical devices, with exposure to global regulatory strategies and high-impact product approvals.