Collaborate with seasoned Systems Engineers on troubleshooting design issues and methods of improvement.
Support all phases of the design and development lifecycle of a medical device
Participate in product design or technical reviews.
Author and review Engineering Change Orders.
Author engineering build requests with direct responsibility for managing engineering materials.
Design and set up feasibility tests in a lab environment.
Author design feasibility protocols and reports.
Participate in product design, technical reviews, and triage brainstorming sessions.
Design verification testing execution in support of design improvements, FDA and international clearance, or commercial release.
Contribute to team goals by accomplishing related tasks as required

BS in an Engineering (Biomedical, Electrical, Computer Science) or similar discipline
Ability to work in a fast paced, dynamic environment with a passion for continuous learning
Passionate about improving the lives of others
Technical writing ability
Experience with lab equipment (testing)
Microsoft office suite (Word, Excel, PowerPoint)
Effective communication skills
1-2 yrs experience as a Systems/Project Engineer in the Medical Device or other regulated industry and/or equivalent
Demonstrated working knowledge of engineering principles and scientific methods.
General understanding of communication, mobile technology, IoT (Internet of Things); a strong plus
Experience with software / product lifecycle tools – Jira, Helix, Bamboo, Bitbucket; a strong plus.
Hands-on and inquisitive, not being afraid to challenge a design
General understanding of medical devices & regulations
Experience with data analysis (MatLAB)
Planning and organization skills
Experience with SolidWorks or Pro-Engineer
Must be able to sit or stand for 8 hours a day

Associate Systems Engineer

Key skills