Hire the best remote EU MDR employees

Discover remote EU MDR workers who are looking for their next full-time, part-time or freelance opportunity on Himalayas.

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16 remote workers

Finding relevant remote workers

Giulia Perotti Ramos@giuliaperottiramos

Netherlands

Regulatory Affairs Coordinator Regulatory Compliance & Operations Regulatory Compliance EU MDR

Regulatory affairs specialist optimizing medical device compliance and operations.

Experience

Project Coordinator III

Current

Medtronic

Jul 2021 - Present (4 years 11 months)

Front Office Receptionist

Hotel Maison Haas Hustinx

Jan 2020 - Jan 2021 (1 year)

Administrative Assistant

Serafin Palestras

Apr 2014 - Jul 2015 (1 year 3 months)

Administrative & Management Assistant

Heineken BR

Nov 2010 - Jun 2013 (2 years 7 months)

Regulatory Affairs Coordinator Regulatory Compliance & Operations Regulatory Affairs Specialist Compliance Manager

Carlos Pérez Barrionuevo@carlosprezbarrionuev

Belgium

And Compliance Engineer Regulatory Affairs Specialist Regulatory Regulatory Strategy

Strategic regulatory leader driving market access for medical devices.

Experience

Rajan sharma@rajansharma4

India

Quality Assurance Medical Devices Compliance ISO 13485 EU MDR

I’m a QA/RA professional driving ISO 13485 and EU MDR Class III compliance.

Experience

Amrita Modak@amritamodak

India

Quality Assurance Compliance Manager Post Approval CMC Activities HAQ

Regulatory Affairs Manager focused on global CTA/IND, EU IVDR/MDR, and CMC delivery for cell & gene therapy and oncology.

Anu Mohan@anumohan

South Korea

Regulatory Affairs Manager Regulatory Strategist Regulatory Strategy Product Registrations

Regulatory affairs specialist experienced in global medical device and SaMD registrations and compliance.

Experience

Omkar Vivek Murtale@omkarvivekmurtale

United States

Regulatory Affairs Specialist Regulatory Affairs Associate 510(K)EU MDR

Regulatory affairs professional ensuring global medical device compliance and streamlined submissions.

Experience

Akhil Menon@akhilmenon

United States

Process Development Engineer Validation Engineer EU MDR Solidworks

Process development engineer specializing in Class III medical devices, validation, and manufacturability improvements.

Experience

Anu Mohan@anumohan1

South Korea

Regulatory Affairs Manager Quality Management Professional Remote Regulatory Affairs

Regulatory affairs professional leveraging global submissions and quality mindset to accelerate medical device compliance.

Experience

Nick Ngankep@nickngankep

France

QEHS Manager Regulatory Affairs Specialist ISO 13485 ISO 9001

Experienced Quality Manager in regulated healthcare and medical devices.

Experience

Anna Moehlmann @annamoehlmann

Switzerland

Quality Assurance Manager Regulatory Affairs Specialist Regulatory Affairs ISO 13485

Regulatory Affairs Specialist and Quality professional driving compliance and continuous improvement for medical devices.

Experience

Manasa R@manasar

India

Regulatory Affairs Quality Assurance EU MDR ISO 13485

I am a Senior Regulatory Affairs engineer advancing global medical device approvals across EU, US, APAC.

Experience

Shahriar Arbabi@shahriararbabi

United States

Post Market Surveillance (PMS) Plans Risk Assessment

Background in clinical medicine, medical research, regulatory affairs, and medical devices.

Experience

Clinical Regulatory Evaluator

National Standard Authority of Ireland

Feb 2022 - Feb 2025 (3 years)

Hilda Njock@hildanjock

Belgium

Pharmacovigilance Specialist Safety Specialist Device Safety Oversight Pharmacovigilance

Medical device safety and pharmacovigilance specialist driving compliance and risk management across product lifecycles.

Experience

Abdul Rahman Ashik@abdulrahmanashik

India

Senior Regulatory Medical Writer Scientific Writer Regulatory Writing Clinical Evaluation

Medical writer specializing in regulatory and scholarly writing with evidence synthesis expertise.

Meghna Roop Raina@meghnaroopraina

India

Microbiologist Regulatory Affairs Quality Management Systems

Regulatory Affairs Executive with expertise in medical devices.

Experience

Executive - Regulatory Affairs

Kendrea Mayes@kendreamayes

United States

Clinical Quality Associate Quality Assurance Engineer Good Clinical Practice (GCP)Good Laboratory Practices (GLP)

Experienced clinical quality professional driving compliance, audit readiness, and continuous improvement in medical devices.

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Hire the best remote EU MDR employees

Finding relevant remote workers

16 remote workers

Finding relevant remote workers

Giulia Perotti Ramos@giuliaperottiramos

Carlos Pérez Barrionuevo@carlosprezbarrionuev

Rajan sharma@rajansharma4

Amrita Modak@amritamodak

Anu Mohan@anumohan

Omkar Vivek Murtale@omkarvivekmurtale

Akhil Menon@akhilmenon

Anu Mohan@anumohan1

Nick Ngankep@nickngankep

Anna Moehlmann @annamoehlmann

Manasa R@manasar

Shahriar Arbabi@shahriararbabi

Hilda Njock@hildanjock

Abdul Rahman Ashik@abdulrahmanashik

Meghna Roop Raina@meghnaroopraina

Kendrea Mayes@kendreamayes

Find top remote talent

Find top remote talent

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Find your dream job

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Find your dream job

16 remote workers

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Giulia Perotti Ramos@giuliaperottiramos

Carlos Pérez Barrionuevo@carlosprezbarrionuev

Rajan sharma@rajansharma4

Amrita Modak@amritamodak

Anu Mohan@anumohan

Omkar Vivek Murtale@omkarvivekmurtale

Akhil Menon@akhilmenon

Anu Mohan@anumohan1

Nick Ngankep@nickngankep

Anna Moehlmann @annamoehlmann

Manasa R@manasar

Shahriar Arbabi@shahriararbabi

Hilda Njock@hildanjock

Abdul Rahman Ashik@abdulrahmanashik

Meghna Roop Raina@meghnaroopraina

Kendrea Mayes@kendreamayes