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Technical Training Specialist, Global Medical Devices

hace 2 meses


Barcelona, Barcelona, España Sgs A tiempo completo

Job Summary

The Technical Training Specialist will be a key member of our team at SGS, responsible for designing, developing, and delivering specialized training programs for our Notified Body, which delivers CE certification services for in-vitro diagnostic medical devices.

Key Responsibilities

  • Support the Training team in preparing and maintaining core training courses related to IVD medical devices, leveraging technical knowledge and collaborating with subject matter experts to ensure training content is effective in achieving defined learning outcomes.
  • Deliver and coordinate the delivery of webinars, workshops, peer-review activities, and other training content.
  • Maintain up-to-date knowledge of relevant medical device regulations.
  • Support and/or deliver external trainings, including administrative support.
  • Assist the Training team in conducting peer reviews and assessment marking for mock audits/technical file reviews.

Requirements

  • 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.
  • Teaching mentoring skills, ability to effectively impart knowledge and support the learning process.
  • Excellent communication skills to convey complex information clearly.
  • Prioritizing the needs and expectations of internal stakeholders.
  • Ability to manage projects and collaborate within a team environment.
  • Establishing and maintaining positive relationships with stakeholders.
  • Strong English literacy.

Desirable Qualifications

  • Good understanding of the EU IVDR and key international standards applicable to medical devices.