Job Description:
We are seeking a motivated and skilledProject Manager to join theGlobal RECON Regulatory Affairs Department. The ideal candidate willhave a strong background in engineering and provenexperience in managing cross-functional projects. Thisrolerequires a proactiveindividual with excellentorganizational and communication skills, capable of drivingresults in a dynamic and regulatedenvironment.
Key Responsibilities
1. Lead and coordinate project activities acrossdepartments to ensuretimely and successfulexecution.
2. Manage project timelines, resources, and deliverables in alignment with company goals with relation to the Market Access activities.
3. Communicateeffectively with stakeholders atalllevels.
4. Monitor project risks and implementmitigation strategies.
5. Prepare and present project reports.
PreferredQualifications
6. Bachelor’s or Master’s degree in Engineering (preferably Management or Biomedical Engineering).
7. Minimum of 3years of experience in project management, ideally in the medical devices industry.
8. Familiarity with MDR (Medical Device Regulation) or similarregulatory frameworks ishighlydesirable.
9. Certification in Project Management is a plus.
10. Proficiency in project management software (e.g., MS Project).
11. Excellentcommand of English (spoken and written).
Key Competencies
12. Problem-solving and decision-making
13. Change management
14. Time management and prioritization
15. Effectivecommunication and negotiation
16. Resilience and reliability
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