Medical Device Engineering Jobs in Alameda, CA

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Regulatory Specialist II  

The Fountain Group LLC - Alameda, California

+ years of regulatory affairs experience Medical Device regulatory affairs experience Job Description: Responsible for regulatory activities, including product registrations, impact assessment, etc

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from: resume-library.com - 5 days ago

Director of Engineering  

SirenOpt - Oakland, CA, United States

inspection systems, electron optics, SEM, lasers, LiDAR, medical devices, optical modeling and simulation, etc. o Proven leadership and project management experience with a track record of managing complex

from: linkedin.com - 2 days ago

Sr Test Engineer – Medical Devices  

Novo - Pleasanton, CA, United States

requirements. Perform thorough evaluation, testing and reporting of medical device products. Understanding and familiarity of ISO 14971 Risk Management Process, IEC 60601-1-6 and IEC 62366 Usability Engineering

from: linkedin.com - 2 days ago

Senior Biomedical Engineer  

Brisbane, CA

-paced engineering team in changing the landscape of medical aesthetics. The Company's technology enables physicians to provide sophisticated solutions for a wide range of medical aesthetic applications

from: Pharmadiversityjobboard.com - 14 days ago

Product Development Engineer  

Gravitas Medical - Berkeley, CA, United States

and assemblies used to manufacture medical devices. • Perform device design reliability engineering activities including test equipment and fixture design, test setup, data analysis and reporting. • Develop

from: linkedin.com - 21 days ago

Lab Manager  

R&D Partners - Redwood City, CA, United States

job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

from: linkedin.com - 2 days ago

Quality Engineer (Medical Device)  

Spirair, Inc. - South San Francisco, California

in the area of quality engineering for medical device manufacturer Working knowledge and application of FDA QSRs and ISO 13485, MDD requirements. Audit experience a plus. BS degree. Excellent communication

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from: resume-library.com (+2 sources) - 17 days ago

Senior Pilot Plant Associate, Process Development  

R&D Partners - Redwood City, CA, United States

in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity

from: linkedin.com - 2 days ago

Director of Manufacturing Engineering  

The Mullings Group - Menlo Park, CA, United States

, and will be proficient in ISO 13485 standards for medical devices. Key Responsibilities: Serve as primary engineering contact for manufacturing partners, ensuring seamless communication and collaboration on Class II IVD

from: linkedin.com - 2 days ago

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Medical Device Engineer  

Griffin Global Systems, Inc. - San Francisco, California

with 1+ years of related experience. Safety testing within IEC 60601 series and IEC 62304 in a medical device environment Safety testing Hardware/development engineering experience Medical Device – highly

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from: resume-library.com - 8 days ago


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