07 ago - Italia
Dormont Manufacturing
Di cosa ti occuperai | What You’ll Do
We are seeking a motivated and skilled Project Manager Market Access to join the Global RECON Regulatory Affairs Department. The ideal candidate will have a strong background in engineering and proven experience in managing cross‑functional projects. This role requires a proactive individual with excellent organizational and communication skills, capable of driving results in a dynamic and regulated environment.
Key Responsibilities
- Lead and coordinate project activities across departments to ensure timely and successful execution.
- Manage project timelines, resources, and deliverables in alignment with company goals with relation to the Market Access activities.
- Communicate effectively with stakeholders at all levels.
- Monitor project risks and implement mitigation strategies.
- Prepare and present project reports.
Preferred Qualifications
- Bachelor’s or Master’s degree in Engineering (preferably Management or Biomedical Engineering).
- Minimum of 3 years of experience in project management, ideally in the medical devices industry .
- Familiarity with MDR (Medical Device Regulation) or similar regulatory frameworks is highly desirable.
- Certification in Project Management is a plus.
- Proficiency in project management software (e.g., MS Project).
- Excellent command of English (spoken and written).
Key Competencies
- Problem‑solving and decision‑making
- Change management
- Time management and prioritization
- Effective communication and negotiation
- Resilience and reliability
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