Medical Device Regulatory Affairs Jobs

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Regulatory Affairs Specialist (Medical Device)  

Qualitest - Fremont, California

regulatory requirements and quality systems. * 3+ years Regulatory Affairs medical device industry experience. * 510(k) experience required, IDE, PMA - optional -(original/revision/supplements) preparation Medical Device Regulatory Affairs Work careers...

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from: resume-library.com - 13 days ago

Regulatory Affairs Manager (Medical Device)  

Qualitest - Fremont, California

as well as external agencies. Also manages the preparation and quality check of all regulatory submissions to regulatory agencies. Requirements * 5+ years of exerience in regulatory affairs within medical Medical Device Regulatory Affairs careers...

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from: resume-library.com - 13 days ago

Principal, Regulatory Affairs - Medical Device  

Naples, Florida

Responsible for managing specific aspects of the Regulatory Affairs program with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in the most efficient regulatory affairs medical devices...

from: Ivyexec.com - 20 days ago

Regulatory Specialist Remote Opportunity  

Gore - Flagstaff, Arizona

on global submissions for implantable medical devices. Responsibilities: Working closely with technical, regulatory affairs, research associates, and product specialists to develop strategies and approaches medical device regulatory affairs certification...

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from: resume-library.com - 2 days ago

Remote Regulatory Affairs Specialist  

Kelly - Sun Prairie, Wisconsin (+1 location)

JOB TITLE: REMOTE REGULATORY AFFAIRS SPECIALIST PAY: $46.03 50.73 PER HOUR DEPENDING ON EXPERIENCE POSITION SUMMARY: Provide technical leadership in the development and implementation of regulatory medical device regulatory affairs consulting...

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from: resume-library.com - Yesterday

Associate Director, Regulatory Affairs, Medical Devices  

San Diego, California

The Associate Director, Regulatory Affairs, Medical Devices provides regulatory guidance and oversight to ensure INOVIO’s compliance with internal SOPs, local, regional, national, and international regulatory affairs specialist medical device...

from: Ivyexec.com - 23 days ago

Director, Quality Assurance Regulatory Affairs  

Gentherm - Cincinnati, Ohio

, complaint handling, Medical Device Reporting, Corrections and Removals, new product development, management reviews, regulatory affairs, and International Product Registration/Approvals. - Formulates virtual medical device regulatory affairs...

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from: resume-library.com - 4 days ago

Regulatory CMC Manager  

Vertex Pharmaceuticals Inc (US) - Boston, Massachusetts

with ability to resolve complex and ambiguous situations * Sound knowledge of cGMP, FDA, EMA, ICH EDUCATION AND EXPERIENCE: * Bachelor's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs medical device regulatory affairs us...

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from: resume-library.com - 4 days ago

Senior Specialist, Regulatory Affairs - Electrical Surgical Medical Devices  

Naples, Florida

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. is actively seeking a Senior Specialist, Regulatory Affairs medical device regulatory affairs senior...

from: Ivyexec.com - 20 days ago

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Program Manager, Regulatory Affairs  

Olympus Corporation of the Americas - Westborough, Massachusetts (+1 location)

to management. *Perform other duties as assigned. JOB REQUIREMENTS REQUIRED QUALIFICATIONS: * Bachelor's degree is required. * Minimum 10 years regulatory affairs experience in the Medical Device industry president medical device regulatory affairs...

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from: resume-library.com (+2 sources) - 5 days ago


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