Design and develop medical devices, equipment, and software that meet clinical and regulatory requirements
Collaborate with cross-functional teams, including physicians, nurses, technicians, and other engineers, to define product requirements and specifications
Conduct feasibility studies, risk assessments, and design verification and validation activities to ensure that products meet regulatory and clinical requirements
Develop and maintain documentation, including design specifications, test plans, and reports, to ensure that products are developed in compliance with regulatory standards
Design and develop software algorithms and applications that support medical devices and equipment
Develop and maintain quality control processes and procedures to ensure that products are manufactured and maintained to a high standard
Participate in the development of clinical trials and studies to evaluate the safety and effectiveness of medical devices and equipment
Strong communication and collaboration skills, with the ability to work effectively in cross-functional teams