Principal Project Manager

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

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Project/Program Management Group

Job Sub Function

Project/Program Management

Job Category

Professional

All Job Posting Locations

Blackpool, Lancashire, United Kingdom, Leeds, West Yorkshire, United Kingdom, West Yorkshire, England, United Kingdom

Job Description

About Orthopedics

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopedics? Ready to join a team that’s reimagining how we heal? Our Orthopedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for a Principal Project Manager role.

Purpose

The Principal Project Manager develops and maintains schedules and priorities for Technical Documentation and Change Notification submissions to Notified Bodies under Regulation (EU) 2017/745 (MDR). Serving as DePuy Synthes' primary point of contact for project planning and execution with Notified Body counterparts, this role provides business teams and Notified Body representatives with clear direction to support timely reviews and achievement of franchise goals.

You will be responsible for:

• Coordinates activities concerned with submissions to EU Notified Bodies including applications and project tracking for new product introduction as well as for changes to existing products.
• Liaises with business units to ensure appropriate execution of submissions.
• Develops andmaintainsdetailed project plans, timelines, and status reports for stakeholders and leadership.
• Identifyproject risks and issues, implement mitigation plans, and escalation asappropriate.
• Coordinates maintenance of MDR Certificate data and associated documentation.
• Represents DePuy Synthes as point of contact for interactions with EU Notified Body with regards to MDR applications, change notifications, TD Assessments and for recurring project and business meetings.
• Establishes accountability for the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.
• Interacts with EU regulatory agency personnel in order to expedite submission and approval of applications as necessary.
• Facilitates relationship building/maintenance with Notified Body by coordinating recurring connections (e.g. weekly, monthly, annual face-to-face meetings)
• Consults with business unit personnel to establish and prepare appropriate priorities for EU regulatory filings for product approvals.
• Supports continuous improvement initiatives byidentifyingopportunities to enhance processes, systems, and project management practices.

Qualifications and Requirements

Education

• Bachelor’s degree requiredin project management, regulatory affairs, life sciences, engineering, ora relatedscientific discipline.

• Master’s degree preferred.

Experience and Skills

Required

• Typically requires 5-8 years of experience in project management, preferably within Medical Device industry
• Proven experience managing cross functional projects in a medical device, or regulated environment
• Strong project planning, scheduling, and organizational skills
• Ability to manage multiple projects simultaneously and meet established deadlines
• Strong communication, collaboration, and stakeholder management skills
• Proficient in MS Office

Preferred

• Experience in supporting new product development and/or product lifecycle management for medical devices.

• Previous experience in project management within a regulatory framework (e.g. submission projects with Notified Body)

• Solid understanding of European Medical Device framework, and quality systems

• Understanding of preparing,submitting, andmaintainingregulatory filings and approvals.

• Excellent written, verbal and presentation skills including experience presenting at meetings with Regulatory Authorities.

• Experience working with global Regulatory Affairs teams and aligning local activities with global strategies.

• Experience using project management and collaboration tools

• Demonstrated ability to manage multiple priorities in a fast-paced environment.

Other

• Languages: English (written and verbal)required.German (written and verbal) is a plus.
• Certifications: Project Management Professional (PMP) or similar certification preferred

Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

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