Latest Medical Device Regulatory Affairs jobs in Alameda, CA

13 Medical Device Regulatory Affairs Jobs in Alameda, CA

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 19 days ago
Regulatory Affairs Specialist – APAC - Diabetes Care (on-site) Abbott Laboratories - Alameda, California . Master’s degree 1+ year of Regulatory Affairs experience within Medical Devices is strongly preferred. Prefer some knowledge of Regulatory history, guidelines, policies, standards, practices, requirements 6 days ago
Product Manager Providence Medical Technology, Inc. - Pleasanton, CA, United States and competitive analysis to identify trends, gaps, and opportunities in the spine medical device sector. Assist in developing and implementing strategic product plans and roadmaps to address market needs. Product 12 days ago
Senior Regulatory Affairs Specialist - Lingo (on-site) Abbott Laboratories - Alameda, California functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for Class II software medical devices Assess the acceptability 5 days ago
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Compliance Manager Abbott Laboratories - Alameda, California Required: Bachelors Degree Minimum 8 years of Quality Systems, Quality Assurance and/or Regulatory Compliance/Affairs experience in In Vitro Diagnostics and medical device manufacturing or other similarly 2 days ago
Senior International Regulatory Product Specialist – Diabetes Care (on-site) Abbott Laboratories - Alameda, California , engineering, or medical fields. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) 2-3 years of experience in regulatory preferred but may consider quality assurance 6 days ago
Regulatory Affairs Specialist – Digital Health Technologies Abbott Laboratories - Alameda, California sciences, mathematics). Master’s degree Experience working in a broader enterprise/cross-division business unit model. Experience working in the Medical Device industry. Regulatory Affairs Professionals 20 days ago
Principal Regulatory Affairs Specialist – Heart Failure (on-site) Abbott Laboratories - Pleasanton, California with Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus. Experience with either 510(k) applications, PMA supplements and US device regulations, or with EU and other 6 days ago
Senior Regulatory Affairs Specialist Nevro Corp. - Redwood City, California from the Regulatory Affairs Professionals Society). Ability to comprehend principles of engineering, physiology, and medical device use. Good analytical thinking skills. Strong communication and regulatory writing 7 days ago
Staff Systems Engineer Abbott Laboratories - Pleasanton, California , Marketing and Regulatory Affairs Preferred Qualifications: Advanced Degree in Engineering (Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline Experience and expertise 2 days ago

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