Latest Medical Device Regulatory Affairs jobs in Lake Forest, CA

12 Medical Device Regulatory Affairs Jobs in Lake Forest, CA

Senior Regulatory Affairs Specialist NeuroVasc Technologies, Inc. - Irvine, CA, United States years’ plus experience in Regulatory Affairs. Experience working with Class I, II and III medical devices. Deep understanding of relevant laws, regulations, and guidelines governing the development 13 days ago
Senior Regulatory Affairs Specialist Intellectt Inc - Irvine, CA, United States Hello Everyone, Greetings of the day. This is Vydehi from Intellectt Inc. We currently have an opening for a Sr Regulatory Affairs Spec with one of our medical device clients. If you or anyone 15 days ago
Manager, Regulatory Affairs - Biosense Webster, Inc. Johnson and Johnson - Irvine, CA fields of study include Engineering, Physical or Biological science or related field. • Minimum 6-8 years of relevant experience with at least five 5 years in Regulatory Affairs of Medical Devices 7 days ago
Principal Regulatory Affairs Specialist MicroVention-Terumo - Aliso Viejo, CA, United States , responsible for submission activities focused on US/EU/Canada and for ensuring compliance to FDA and international regulatory agency requirements for Neurovascular and Peripheral medical devices. What You'll 15 days ago
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Planning Analyst Insight Global - Irvine, CA, United States . This person will be responsible for working with regulatory affairs, Research & Development, Supply Chain, and Quality to support franchise projects concerning one medical device unit, planning integration, etc 15 days ago
Director, Global Regulatory Affairs – Soft Tissue Fillers MPS AbbVie - Irvine, California (new equipment, aseptic fill, clean rooms) Assist the team in supporting regulatory interactions with Quality, Medical Safety and International Regulatory Affairs colleagues. Provides regulatory policy 23 days ago
Quality Inspector (3rd shift) Applied Medical - Rancho Santa Margarita, California processes. Gain familiarity with the production environment and key stakeholders. Perform initial inspections of medical devices under supervision. Begin documenting inspection results and maintaining 10 days ago
Engr 3, Product Development, La Brea CA Stellar Consulting Solutions - Brea, CA or as part of a cross-functional team with members from marketing, sales, clinical, regulatory, medical affairs, quality, manufacturing, etc. Experience with medical device design control processes $Based on experience 22 days ago
Analyst, Market Implementation Applied Medical - Rancho Santa Margarita, California to meet all hospital credentialing requirements, which may include background check, drug screen and vaccinations Preferred: The following skills and attributes are preferred: Medical Device, Product 14 days ago
Manager of Tech Investigation Fujifilm - Santa Ana, California Service and/or Quality Assurance/Regulatory Affairs/Compliance, technical and customer support in a medical device discipline. Two (2) or more years of direct supervisory or management experience. GMPs 7 days ago

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