Medical Device Regulatory Affairs Jobs in Rancho Santa Margarita, CA

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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

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from: resume-library.com - 9 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

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from: resume-library.com - 13 days ago

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

from: linkedin.com - 12 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

from: linkedin.com - 14 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

from: Johnson and Johnson - 6 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

from: linkedin.com - 14 days ago

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

from: linkedin.com - 14 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

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from: resume-library.com - 22 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

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from: resume-library.com - 6 days ago

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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

from: Dice.com - 21 days ago


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