Technical Training Specialist

hace 5 horas

Madrid, Madrid, España SGS A tiempo completo

The role of Technical Training Specialist, Global Medical Devices, is a key position within our team at SGS. The successful candidate will be responsible for the design, development, and delivery of specialized training programs for our Notified Body, which delivers CE certification services for in-vitro diagnostic medical devices.

Key Responsibilities:

  • Training Course Preparation: Collaborate with the Training team to prepare and maintain core training courses related to IVD medical devices.
  • 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.

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.
  • IT literacy.
  • Establishing and maintaining positive relationships with stakeholders.
  • Strong English literacy.

Desirable:

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

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