Technical Training Specialist for Medical Devices

hace 3 días


Madrid, Madrid, España Sgs A tiempo completo
Job Description

The Technical Training Specialist will play a key role in our team, responsible for designing, developing, and delivering specialized training programs for our Notified Body, which provides CE certification services for in-vitro diagnostic medical devices.

As part of the Global Medical Device Training Team, you will support the training needs of our dynamic and rapidly growing team of experts, covering broad-ranging topics including the clinical and technical aspects of IVD assays, the regulatory requirements of the EU In-vitro Diagnostic Medical Device Regulation, as well as relevant guidance documents and standards (ISO 13485, ISO 14971, various CLSI guidance, etc.).

This role is integral to ensuring that our team possesses the necessary skills and knowledge for effective conformity assessments in the ever-evolving landscape of medical device regulations.

The Global Medical Devices Technical Training Specialist contributes to the ongoing competence and professional development of the team, thereby enhancing the overall capabilities of the Notified Body.

Key Responsibilities:
  • Training
  • Course Preparation: Support the Training team in preparing and maintaining core training courses related to IVD medical devices, leveraging your own technical knowledge as well as collaborating with subject matter experts to ensure training content is effective in achieving the defined learning outcomes
  • Training Delivery: Deliver and coordinate the delivery of webinars, workshops, peer-review activities, and other training content
  • Regulatory Knowledge: Maintain up-to-date knowledge of relevant medical device regulations
  • External Training Support: Support and/or deliver external trainings, including administrative support
  • Peer Reviews and Assessments: Assist the Training team in conducting peer reviews and assessment marking for mock audits/technical file reviews
Qualifications:
  • Experience in the field of in vitro diagnostic medical devices gained in the IVD industry, clinical diagnostics laboratory, relevant research, IVD regulatory affairs, or other relevant professional setting
  • Bachelor level education, preferably in engineering, science, or a healthcare-related domain
  • IT literacy
  • Proven experience in progressively training technical skills, preferably within multinational organizations both in online and face-to-face methodologies
Desirable:
  • Good understanding of the EU IVDR and key international standards applicable to medical devices


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