1. Engineers: These include biomedical engineers, mechanical engineers, electronic engineers, etc., who are responsible for the design, development and maintenance of medical devices.
2. Quality control specialists: they are responsible for testing and verifying the performance and quality of medical devices to ensure that they meet relevant standards and regulatory requirements.
3. Clinical experts: doctors, nurses and other medical personnel who have extensive clinical experience in the use of medical devices, and can provide assessment and advice on the devices in actual clinical applications.
4. Safety evaluation experts: responsible for risk assessment and safety evaluation of medical devices to ensure that their use will not cause harm to patients and operators.
5. Certification Auditor: Responsible for auditing the medical device company's quality management system and related documents to ensure compliance with certification standards such as ISO.
It is important to note that the exact composition of the technical staff may vary depending on the size of the company, the scope of the business and the type of product. Further consultation with the medical device company or relevant management is recommended in specific cases.