Project Manager, Mediterranean

DePuy Synthes is recruiting for a Project Manager Mediterranean in Regulatory Affairs located in Maroussi AthensAttiki

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 ascrossfunctionalstakeholders 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 ensureontimedelivery of regulatory submissions and related activities.

• Coordinatecrossfunctionalteams 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

• Bachelors degree preferably in Life Sciences Engineering Regulatory Affairs ora relateddiscipline.

• Advanced degree (e.g. Masters) 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 managingcrossfunctionalprojects 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 andproblemsolvingskills.

• Clear professional communication skills both written and verbal.
  

Other:

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

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

• Certifications:Project management certification preferred not.