6 medical device engineer jobs at 4 companies in Carmichael, CA
3w
Save
Mark Applied
Hide
3w
Field Service Engineer 2H (Medical Device) (Sacramento, CA based Field role))
Sacramento or Chicago or Minneapolis
$1-$100000k/hrFieldFull Time
HaemoneticsNYSE: HAE: Manufactures medical devices for blood and plasma management.
5+ YOE5-8 years field service experience with medical devices, BS or technical certificate preferred, ability to travel up to 75%, strong troubleshooting, documentation, communication, and customer-service skills.
PenumbraNYSE: PEN: Designs and manufactures medical devices for vascular conditions.
2+ YOEAssociate’s or Bachelor’s in engineering/life science,2+ years quality engineering experience (medical device environment preferred),familiarity with QSR/ISO,excellent communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
PenumbraNYSE: PEN: Designs and manufactures medical devices for vascular conditions.
7+ YOEBachelor's in engineering required; 7+ years quality or manufacturing engineering in medical device; expert with FDA QSR and ISO 13485; Lean/Six Sigma experience; advanced statistical and DOE skills; ASQ CQE/CSSBB preferred.
DanaherNYSE: DHR: Develops scientific instruments and diagnostic tools for healthcare markets.
3+ YOEBachelor’s in Microbiology, Biomedical Engineering, or related field with 3+ years experience, or Master’s with 0+ years; experience in regulated manufacturing (medical device/pharma); strong root-cause analysis and problem-solving; good communication; cross-functional collaboration.
DanaherNYSE: DHR: Develops scientific instruments and diagnostic tools for healthcare markets.
8+ YOE8+ years tooling and automation engineering experience, degree in mechanical/plastics/polymer or equivalent, expertise in tooling/fixture design, automation equipment development, vendor management, equipment qualification, and medical device/process validation.
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
7+ YOEBS in Molecular Biology, Genetics, or Engineering required; PMP preferred. 7+ years program management experience with regulated medical device or similar products; budget, risk, timeline, and external partner management; strong communication and financial skills.