Medical Device Regulatory Affairs Jobs

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Senior Content Writer  

Clarivate - Baltimore, MD, United States

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed...

from: linkedin.com

Clinical Evaluation Report Medical Writer  

Criterion Edge - San Luis Obispo, CA, United States

Combine understanding of scientific and research methodology, medical device regulations and guidelines, and product knowledge, to...

from: linkedin.com

Regulatory Affairs Specialist (Remote Optional)  

BD - Webb City, Missouri, us

to legally market medical devices in the European Union under the MDR. This role will provide support for global product registrations and related regulatory affairs activities, as required. This role Medical Device Regulatory Affairs Work careers...

from: talent.com - 4 days ago

Senior Quality Systems Specialist - Medical Devices - REMOTE  

CyberCoders - Cleveland, OH, United States (+8 locations)

during internal and external audits What You Need for this Position Bachelor's degree in related field 5+ years in the medical device industry Quality Systems (Quality Planning / Management Review Medical Device Regulatory Affairs careers...

from: linkedin.com - Yesterday

#2691 - SOP Writer/Tech Writer  

Qualitest - Raleigh, NC, United States

data, and communicating outputs. Experience working within a medical device or pharmaceutical organization in a Research & Development, Scientific and Medical Affairs, Clinical or Regulatory role regulatory affairs medical devices...

from: linkedin.com (+1 source) - 5 days ago

Associate Director/ Director, Regulatory Affairs - PCR Core Labs  

QIAGEN - Ann Arbor, Michigan

role, responsible for successful pre-market submissions. Extensive knowledge of regulatory requirements and processes for US, Canada, and EU commercialization of IVD medical devices (RoW knowledge medical device regulatory affairs certification...

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from: resume-library.com - Yesterday

Senior Project Manager (QMS, Med-Tech) - REMOTE  

CyberCoders - San Diego, CA, United States (+7 locations)

with quality systems and/or regulatory affairs Understanding of US & International medical device regulations Management of QMS related compliance or improvement projects Foundational QMS processes (NC/CAPA medical device regulatory affairs consulting...

from: linkedin.com - 3 days ago

Regulatory Affairs Specialist - Remote  

Cook Group - Bloomington, Indiana (+1 location)

medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook regulatory affairs specialist medical device...

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from: resume-library.com - 2 days ago

VP Clinical & Regulatory Affairs  

Senseye - Austin, Texas

President of Clinical & Regulatory Affairs to manage the clinical and regulatory operation strategy and tactical implementation of pre-clinical, pivotal, and post-market studies for our class II & class III virtual medical device regulatory affairs...

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from: resume-library.com (+1 source) - Yesterday

Sr. Regulatory Affairs Specialist  

BD - Covington, Georgia, us

. and European medical device regulationsMust have technical writing skills and be proficient at compiling successful submissions for the appropriate audienceEDUCATION and/or EXPERIENCE:BS in a Scientific Field medical device regulatory affairs us...

from: talent.com - 4 days ago

Regulatory Affairs Specialist I - Hybrid  

Cook Group - Bloomington, Indiana

medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook medical device regulatory affairs senior...

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from: resume-library.com - 2 days ago

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Regulatory Scientist  

Cook Group - West Lafayette, Indiana

requirements applicable to the performance of regulatory affairs tasks related to pre-market submissions for medical devices, with specific expertise in either European or US requirements. Excellent oral president medical device regulatory affairs...

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from: resume-library.com - 2 days ago


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