Job Responsibilities
- Help in the creation of clinical procedure materials such as procedure guides, set-up cards, and clinical videos to enable training to both internal and external customers.
- Help in collaborating across the company as needed, but especially regulatory; human factors and usability; and quality to ensure that the respective indications are aligned with the regulatory objectives.
- Support the translation of clinical need into actionable engineering requirements and vice versa.
- Help in the creation of Clinical Design Validation Protocols & Reports.
- Develop user manual and training documentation.
- Perform other ad-hoc tasks / projects as assigned.
- Develop user manual and training documentation.
Job Requirements
- Bachelor or above in Biomedical Engineering or relevant field. Fresh graduate would also be considered.
- Affinity with clinical environment and medical device.
- A good understanding, and preferably proven experience, of the medical product development process as relates to the development of surgical devices in a regulated environment.
- Strong problem-solving skills and interpersonal skills.
- Fluency in written and spoken English & Mandarin is mandatory.