DePuy Synthes is recruiting for a(n) Project Manager, Nordics,locatedinOstbanegade 123, Copenhagen, Denmark

Johnson & Johnson announced plans to separate our Orthopedics business toestablisha standalone orthopedics company,operatingas DePuy Synthes.The process of the planned separation isanticipatedto be completed within 18 to24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may berequired, regulatory approvals and other customary conditions and approvals. Should you accept this position, it isanticipatedthat, following conclusion of the transaction, you would be an employee of DePuySynthesand your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes atan appropriate timeand subject to any necessary consultation processes.

The Project Manager, Nordics,supports the planning, coordination, and delivery ofQARA‑relatedprojects across the Nordic marketsThis role plays a keypartin enabling compliant,timelymarket access and business continuity by coordinating cross‑functional initiatives related to regulatory compliance, quality system execution, and operational readiness.

This position offers broad exposure to regional and global stakeholders and the opportunity to make a tangible impactina highly regulated MedTech environment by supporting quality and regulatory excellence across the Nordics.

Key Responsibilities

• Plan, coordinate, and manage QARA‑related projects supporting regulatory compliance, quality system activities, and market readiness across Nordic countries.

• Develop andmaintainproject plans, timelines, milestones, dependencies, and risk registers aligned with QARA and businessobjectives

• Coordinate cross‑functional teams including Quality Assurance, Regulatory Affairs, Supply Chain, Operations, and Commercial partners.

• Track project progress,identifyrisks or issues, and drivetimelymitigation and resolution in collaboration with stakeholders.

• Support implementation of local market initiatives related to regulatory submissions, lifecycle management, audits, and quality system activities.

• Ensure project activitiescomply withinternal policies, quality management system requirements, and applicable regulatory standards.

• Prepare and deliver project status updates, dashboards, and communications for QARA leadership and key stakeholders.

• Contribute tocontinuous improvement initiatives to enhance project execution, QARA processes, and local market support effectiveness.

• Ensuring proactive engagement and shaping of regional policy initiatives that are critical to business strategy, continuity, and growth.

Qualifications

Education

• Required:Bachelor’s degree in Business, Life Sciences, Engineering, Regulatory Affairs, ora relatedfield.

• Preferred: Advanced degree or project management certification (e.g., PMP, PRINCE2) or training in quality/regulatory disciplines.

Experience and Skills

Required:

• 4–6 years of progressive experience in project management, quality, regulatory support, operations, or a related role within a regulated industry.

• Experience managing cross‑functional projects with multiple stakeholders in a matrixed environment.

• Strong organizational, planning, and documentation skills with high attention to detail.

• Ability to manage multiple priorities and deadlines in a dynamic environment.

• Strong written and verbal communication skills, including stakeholder reporting.

• Proficiency with standard project management and office tools.

Preferred:

• Experience supporting Quality Assurance and/or Regulatory Affairs activities.

• Familiarity with medical devices, healthcare, or other highly regulated industries.

• Exposure tointernationalor multi‑country market models.

• Experience working in a multinational or matrixed organization.

• Project management certification (e.g., PMP, PRINCE2, Agile).

Other

• Language: English required; Nordic language(s) preferred.

• Travel: Limited to moderate regional travel within the Nordics.

• Certifications: Project management certifications preferred but not required.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com

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