Technical Training Specialist for Medical Devices
4 weeks ago
About SGS
SGS is the world's leading testing, inspection, and certification company. We are recognized as the global benchmark for sustainability, quality, and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer, and more interconnected world.
Job Summary
The Technical Training Specialist will be a key member of our team, 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
- Training Course Preparation: 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 effective training content.
- 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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