Effective design, development, and project engineering
Engage physicians, patients, sales reps, marketing, and others to collect feedback for devices under development
Deliver meaningful innovation and submit novel intellectual property
Create specifications and perform engineering analyses
Design for cost-effective manufacturability
Develop and analyze project scopes and schedules
Define and validate manufacturing processes, support engineering builds, and verify product performance.
Train and mentor entry-level engineers
Stay abreast of emerging technologies, trends, and competition.
Deliver designs that meet goals such as performance, standards, manufacturability, reliability, and cost.
Generate regulatory audit worthy design and risk management documentation
Minimum qualifications:
Experience as a hands-on design and project engineer in the medical device industry, responsible for new implantable and external device designs, materials, equipment, and processes.
Education in Mechanical or Biomedical engineering with a B.S. and 7+ years of experience or M.S. and 5+ years of work experience.
Hands-on experience utilizing SolidWorks 3D CAD and drafting standards (e.g., ANSI Y14.5)
Experience executing projects through commercial launch
Preferred qualifications:
Experience involving/supporting
Implantable leads, implantable pulse generators, surgical tools, access instruments, or handheld and wearable devices
Materials biocompatibility
Animal studies, preclinical studies, cadaver lab, field research and clinical studies to evaluate the usability and performance of designed products