Medical Device Regulatory Affairs Jobs in Irvine, CA

Bright Uro - Irvine, CA, United States

Uro markets, including Registration, Non-Conformities, Product Recalls, Field Actions and Medical Device Reporting. Maintain and update regulatory files and binders. Education and Work Experience

from: linkedin.com - 13 days ago

Redbock - an NES Fircroft company - Irvine, CA, United States

+ years in medical device regulatory affairs Understanding of current FDA and International regulations, guidance and standards applicable to medical device products Excellent written and verbal

from: linkedin.com - 11 days ago

AbbVie - Irvine, California

relationships with relevant stakeholders including Regulatory Affairs functional areas, Precision Medicine, Medical Affairs and Commercial organizations. Represents CDx Device RA on teams to negotiate, influence

from: resume-library.com - 9 days ago

Willow Laboratories - Irvine, CA, United States

Compliance: Ensure compliance with all relevant regulatory standards and requirements for medical devices during the manufacturing process. Collaborate with regulatory affairs to obtain necessary

from: linkedin.com - 6 days ago

Nihon Kohden America - Irvine, CA, United States

, or related discipline 2+ years of experience in regulatory affairs within the medical device space Demonstrated proficiency with global regulatory planning and strategy for submission preparation (including

from: linkedin.com - 11 days ago

Fujifilm - Santa Ana, California

educational degrees (Masters or PhD) are desirable and may count towards experience. Five (5) or more years of experience in Technical Support or Customer Service and/or Quality Assurance/Regulatory Affairs

from: resume-library.com (+1 source) - 4 days ago

NeuroVasc Technologies, Inc. - Irvine, CA, United States

: Bachelor’s degree or higher in Life Sciences, Engineering, or related disciplines. Minimum of 5 years’ plus experience in Regulatory Affairs. Experience working with Class I, II and III medical devices. Deep

from: linkedin.com - 10 days ago

HCLTech - Irvine, CA, United States

in product design Regulatory requirement Certification such as RAC (Regulatory Affairs Certification) is often preferred Preferred Qualifications Quality or Regulatory compliance experience Experience

from: linkedin.com - 10 days ago

Katalyst Healthcares & Life Sciences - Brea, California

, medical affairs, quality, manufacturing, etc. Experience with medical device design control processes and creating and maintaining design control documentation

from: resume-library.com - 2 days ago

Meet - Irvine, CA, United States

, root cause analysis, risk analysis, risk mitigation, sampling, and control plans. Collaborate closely with Quality System, Manufacturing Quality, and Regulatory Affairs partners to maintain a fully

from: linkedin.com - 11 days ago