Latest Medical Device Regulatory Affairs jobs in Irvine, CA

19 Medical Device Regulatory Affairs Jobs in Irvine, CA

Regulatory Affairs Consultant Redbock - an NES Fircroft company - Irvine, CA, United States A fast-growing orthopedic Medical Device company in Irvine, CA is in immediate need of a Regulatory Affairs Consultant to support them for approximately 3 months . The consultant will need to work 4 days ago
Manager, Regulatory Affairs - Medical Devices Allergan Aesthetics - Irvine, California Represents US Regulatory in project teams. Develops US regulatory filing strategy, with input from supervisor. Provides regulatory... 10 days ago
Regulatory Affairs Specialist Kelly Science, Engineering, Technology & Telecom - Irvine, CA, United States Regulatory Affairs Specialist (hybrid) Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA 11 days ago
Regulatory Affairs Specialist - Contract 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 4 days ago
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Manager Regulatory Affairs, In Vitro Diagnostics and Companion Diagnostics (Remote) 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 9 days ago
Sr Regulatory Affairs Motion Recruitment - Irvine, CA, United States Our client, is a Fortune 100 medical device company that specializes in critical care technology, structural heart innovation, and surgical monitoring. They have a long-standing culture of integrity 7 days ago
Quality Specialist ( Audit & Regulatory ) 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 11 days ago
Regulatory Affairs Specialist, Selution (Irvine, CA) Cordis - Irvine, California /Biomedical/Pharmacy or equivalent professional experience. • 2+ years of experience in regulatory affairs in medical device/pharmaceutical industry, GLP, ISO 13485 environment • Experience in FDA / EU 12 days ago
Senior Regulatory Affairs Specialist 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 22 days ago
Regulatory Specialist 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 22 days ago

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