Medical Device Product Management Jobs in Alameda, CA

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

from: resume-library.com - 12 days ago

Ursus, Inc. - Alameda, California

and process improvements Performs other related duties and responsibilities, as assigned Qualifications: 4+ years of medical device (class II and III) industry experience 2+ years' experience in quality system

from: resume-library.com - 14 days ago

Openwater - San Francisco, CA, United States

the Role As a VP of Manufacturing at Openwater, you will be responsible for the development of our contract manufacturing pipeline for our next generation medical components and devices. This includes

from: linkedin.com - 7 days ago

Bone Health Technologies - Redwood City, CA, United States

preferred. Minimum of 15 years of progressive leadership experience in operations management within the medical device industry. Proven track record of success in driving operational excellence, implementing

from: linkedin.com - 23 days ago

Abbott Laboratories - Pleasanton, California

of 4 years’ experience in a Marketing Product Management role Preferred Qualifications: MBA or Master's Degree Experience with Design Thinking or Bio Design methodology Class III medical device

from: resume-library.com - 6 days ago

Providence Medical Technology, Inc. - Pleasanton, CA, United States

, Marketing, Engineering, or a related field. Advanced degree (MBA, MS) preferred. Minimum of three (3)+ years of product management experience in the medical device industry, with a strong preference

from: linkedin.com - 6 days ago

Randstad Life Sciences US - Menlo Park, CA, United States

in accordance with our medical device and clinical laboratory quality management system requirements. This person works closely with Supply Chain, Manufacturing Science & Technology (MSAT), Quality Control (QC

from: linkedin.com - 6 days ago

Pfizer - San Francisco, CA

of all MDCP lifecycle documentation including design controls, risk management, quality management systems, change controls, vendor management, product release and complaints. Ensure device design, development USD 161,600.00 - 269,400.00 per year

from: Dice.com - 17 days ago

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 - 9 days ago

The Mullings Group - Menlo Park, CA, United States

companies/product lines Demonstrated knowledge of FDA regulations for Class II IVD products and proficiency in ISO 13485 medical devices quality management systems Proven track record of managing cost

from: linkedin.com - 9 days ago