DePuy Synthes is recruiting for a Project Manager Mediterranean in Regulatory Affairs located in Maroussi– Athens,Attiki

The Project Manager, Mediterranean in Regulatory Affairs plays a critical role in planning, coordinating, and delivering regulatory projects that support DePuy Synthes’ product portfolio across the Mediterranean region. This role partners closely with regional and global Regulatory Affairs teams, as well ascross‑functionalstakeholders, to ensure regulatory activities are executed on time, within scope, and in compliance with applicable regulations. The position offers the opportunity to drive meaningful impact by enablingtimelymarket access and lifecycle management of innovative orthopedic solutions.

Key Responsibilities

• Plan, coordinate, and manage Regulatory Affairs projects across the Mediterranean region in alignment with business and regulatoryobjectives

• Develop andmaintainproject plans, timelines, and milestones to ensureon‑timedelivery of regulatory submissions and related activities.

• Coordinatecross‑functionalteams, including Regulatory Affairs, Quality, Clinical, Supply Chain, and Commercial partners.

• Monitor project risks, dependencies, and resource needs; proactively escalate issues and propose mitigation plans.

• Ensure project executioncomplies withregional and international regulatory requirements, policies, and procedures.

• Track and communicate project status, deliverables, and key metrics to regional and global stakeholders.

• Support continuous improvement of regulatory project management processes and tools.

Qualifications

Education

• Bachelor’s degreerequired, preferably in Life Sciences, Engineering, Regulatory Affairs, ora relateddiscipline.

• Advanced degree (e.g., Master’s) preferred.
  

Experience and Skills

Required:

• Several years of relevant experience in Regulatory Affairs, project management, or a related function within a regulated industry (medical devices preferred).

• Demonstrated experience managingcross‑functionalprojects with multiple stakeholders.

• Working knowledge of regulatory requirements and processes applicable to medical devices.

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

Preferred:

• Experience supporting regulatory activities across multiple countries or regions.

• Familiarity with EU and Mediterranean regulatory frameworks for medical devices.

• Formal project management training or certification (e.g., PMP, PRINCE2).

• Experience working in a matrixed, global organization.

• Proficiencywith project management tools and reporting dashboards.

• Strong organizational, planning, andproblem‑solvingskills.

• Clear, professional communication skills, both written and verbal.
  

Other:

• Languages:Fluency in Englishrequired;additionalMediterranean languages are an advantage.

• Travel:Moderate.Ability to travel regionally and internationally asrequired(estimated up to 20%).

• Certifications:Project management certification preferred, notrequired