5 medical device engineer jobs at 5 companies in Flint, MI
2w
Save
Mark Applied
Hide
2w
Engineer, Process/Validation
Fraser, Michigan, United States
$75k-$94k/yrHybridFull Time
GetingeNasdaq Stockholm: GETI B: Manufactures medical equipment for acute care and life sciences.
3+ YOEBachelor's in engineering, minimum 3 years medical device experience, knowledge of IQ/OQ/PQ, pFMEA, process validation, regulatory quality compliance, and strong written communication.
TriMasNASDAQ: TRS: Manufactures engineered products for packaging, aerospace, and industrial markets.
5+ YOE5+ years plastics or manufacturing experience; SolidWorks desired; ISO/medical device and injection molding experience desirable; bachelor's in related discipline preferred; Six Sigma/Lean training preferred.
Leo Cancer Care: Field Service Engineer Level I-III
Flint, Michigan, United States
FieldFull Time
Centaur Health Holdings: Developing innovative radiotherapy and veterinary diagnostic imaging solutions.
Provide on-site installation, troubleshooting, maintenance and repair of electro-mechanical medical devices; reside within ~75-mile radius of Flint, MI; willing to travel up to 40%; valid driving license; MS Office and Salesforce experience beneficial.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Salesforce
Corza Medical: Manufacturer of surgical instruments and specialized wound closure devices.
2+ YOEBachelor's in engineering, 2+ years medical device manufacturing experience, knowledge of FDA QSR (21 CFR 820) and ISO 13485, process validation, SolidWorks and Labelview proficiency, MS Office skills, root cause analysis; US work authorization required.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, SolidWorks, Labelview, AutoCAD
Mounds View or Grand Rapids or Dexter or Brooklyn Park or United States
$171k-$257k/yrHybridFull Time
MedtronicNYSE: MDT: Developing and manufacturing medical technologies and therapies globally.
5+ YOEBachelor's degree in engineering, quality, life sciences, business, or a related technical field; 5–7+ years of relevant experience in a regulated industry. Medical device and quality program experience preferred.