6 device development jobs at 3 companies in Portage, MI
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Staff Software Systems Engineer- Medical Device
Portage or Grand Rapids
$103k-$171k/yrHybridFull Time
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
4+ YOEBachelor's in software engineering/computer science and 4+ years' experience; experience with requirements management, system modeling, SDLC/ALM traceability, verification/validation, and medical device regulatory knowledge.
Aspen Surgical: Manufactures and supplies disposable surgical and medical instruments.
10+ YOE5+ MgmtBachelor's in engineering/biomedical, 10+ years medical device product development including 5+ years leading teams; proven FDA-cleared launches, design control/21 CFR Part 820/ISO 13485 knowledge, stage-gate and project management experience.
enFocus: Drives regional growth through talent attraction and innovation projects.
Undergraduate, graduate, or recent graduate eligible; strong communication, leadership, project management, research and analytic skills; familiarity with business/data analytics; available full-time for 8 weeks in South Bend-Elkhart region; must provide own device and transportation.
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
6+ YOEBachelor's degree, 6+ years experience, 40% travel, MBA and medical device/New Product Development experience preferred; strong presentation and cross-functional skills.
LCS: A senior living community employer providing programs and services to support residents' social, emotional, and daily living needs.
2+ YOE2 years experience in geriatrics/recreation or related degree preferred; college degree preferred; Microsoft Office and smart device proficiency; ability to develop programs and manage resident communications.
Microsoft Office, Amazon Echo, Go Icon, Jotform, Facebook
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
2+ YOEBachelor's in Mechanical Engineering, minimum 2 years product development/mechanical design experience, CAD/Creo proficiency preferred, medical device or regulated industry experience, knowledge of design controls and verification testing.