Working within a team to identify and implement effective controls to support development and maintenance of products to meet internal and external requirements
Developing understanding of Design Controls, Risk Management and Usability for Medical Devices
Applying repeatable problem-solving concepts
Keeping abreast of standard practices
Supporting departmental, functional, and divisional design quality goals and priorities.
Building quality into all aspects of work by maintaining compliance to all quality requirements
Participating in various design quality assurance and compliance improvement projects
Other duties as necessary or required by the organization
Required qualifications:
Bachelor’s degree in Biomedical Engineering, Mechanical, Electrical Engineering or related field of study
1+ year of related work experience from Medical Device Industry
Demonstrated interpersonal skills with ability to work within a team environment