Specjalista / Specjalistka ds. certyfikacji wyrobów medycznych (biomateriały)
Core
Coordinating medical device certification processes to ensure technical documentation compliance with EU Regulation 2017/745 for biomaterials and implants.
Role type
Medical Device Certification Specialist (Biomaterials)
Builds
Certification compliance for orthopedic implants, dental implants, and biomaterials
Domain
Medical Devices / Regulatory Compliance
Deliverable
client delivery
Required skills
EU Regulation 2017/745 knowledge, technical documentation review, stakeholder coordination, audit participation, time management, MS Office
Preferred skills
Experience with implantable medical devices, knowledge of implantable device regulatory requirements
Technologies
MS Office
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