Top Freelance European Medical Device Regulation (MDR) Experts For Hire

Ilkay K.

EU MDR Specialist with years of QMS experience working with companies like Tüv and Dekra as Lead Auditor
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USD 50/hr
Master of Communication in Digital Media
Germany

20+ years of QMS experience, ISO 9001 Lead Auditor, ISO 14001, ISO 13485. Heading currently a team of MDR consultant in Germany and providing M...

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USD 50/hr
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Ben C.

Therapeutic Goods Consultant: Quality Systems, Regulatory Affairs, Auditing, Product Development and Validations
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USD 150/hr
Diploma in Quality Auditing
Australia

I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...

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USD 150/hr
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Neethu A.

Medical Device Regulatory Specialist - U.S. FDA, 510(k), Specialized at Polymer glove 510(k) documentation
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USD 50/hr
Applied Electronics
India

Medical Device Regulatory Specialist with years of experience and a deep understanding of European and FDA medical device regulations. Investig...

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USD 50/hr
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Soundarya P.

Scientific writer with 3+ years of hands-on experience in developing and reviewing clinical evaluation reports-MDD&M...
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USD 45/hr
Masters of Pharmacy
India

Handled more than 30 clinical evaluation reports end to end, starting from clinical evaluation plan, literature screening, literature summaries...

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USD 45/hr
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ADNAN A.

QA/RA Medical Devices Expert
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USD 150/hr
BEng Hons Manufacturing Engineering
United Kingdom

20 years in Medical Devices, QA. RA, Validation for all Classifications of Medical Devices. MDR. IVDR expertise, with Software as a Medical Dev...

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USD 150/hr
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Caique M.

- Post-market surveillance Analyst - Medical writer with experience in CER and PMS.
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USD 80/hr
Bachelor in Biomedicine
Brazil

I am a freelance science and medicine writer, my focus is on implantable medical devices related to the areas of orthopedics. I specialized in ...

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USD 80/hr
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Viky Gilles Daniel V.

Global Regulatory Affairs Consultant - FDA - Medical Device - Pharma
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USD 150/hr
Global Regulatory Affairs Certification
United States

Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...

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USD 150/hr
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Kristen H.

Medical Writer with 5+ years of experience in systematic literature review, marketing, medical content writing
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USD 45/hr
MA Athletic Training
United States

As a seasoned medical technical writer and chronic illness patient advocate, I am devoted to the meticulous translation of intricate medical in...

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USD 45/hr
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Andrew B.

Medical writer with 4+ years of experience in clinical evaluation
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USD 50/hr
Master of Public Health
United States

Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...

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USD 50/hr
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Mariem R.

Study Start Up Specialist France | Sr CRA Medical | PMCF
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USD 100/hr
Master of Public Health
France

I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...

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USD 100/hr
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Assaf G.

Medical devices professional with more than 25 years' experience in senior management positions.
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USD 150/hr
MSc.
Israel

Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...

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USD 150/hr
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Anil C.

Over 25 years of experience as a Medical Device Regulatory Consultant | CDSCO | USFDA 510k | EU MDR CE Marking | SFDA |
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USD 300/hr
M.Sc. Microbiology
India

Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...

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USD 300/hr
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William T.

Writer and Scientist skilled in project management, compliance, and high-throughput automation within CL3 environments.
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USD 40/hr
MSc - Infection and Immunity
United Kingdom

Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...

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USD 40/hr
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Manoj Krishnaa S.

EU MDR consultant | Medical device QA RA
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USD 8/hr
B.Tech
India

I help clients to define the medical device documents and align with Regulatory aspects. Works with small business owners and entrepreneurs. T...

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USD 8/hr
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Elaine S.

Freelance Medical Writer | Expertise in Orthopaedic Medical Devices
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USD 50/hr
Excercise and Sport Physiology - Biomechanics
United States

Extensive experience in orthopedic biomedical research, data analysis, manuscript writing and editing, CEP/CER writing for EU MDR, and systemat...

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USD 50/hr
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Ranjith P.

Medical Device Regulatory (Expert in Creating Technical documentation as per MDD 93/42/EEC/MDR 2017/745, CE marking)
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USD 75/hr
Masters Degree
United Kingdom

• Prepare Technical documentation for Medical Device CE marking • Support MDR Compliance execution by reviewing/updating/creating Technical doc...

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USD 75/hr
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Kalidoss P.

https://www.linkedin.com/in/kalidoss-p-09353a65
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USD 10/hr
Biomedical Engineering
India

Work experience in Medical device regulatory, cybersecurity of the medical device, clinical evaluation report analysis, risk benefit analysis.

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USD 10/hr
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Chunnan C.

Passionate MedTech innovator with a startup mentality, devoted to application and clinical development of novel techs
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USD 90/hr
Life Science, B.Sc.
Germany

An experienced professional with 20 years of industrial experience in MedTech, biopharmaceutical companies and semi-governmental organizations;...

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USD 90/hr
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Michael L.

R&D Expert; Specializing in Laser Systems, IVF Microscopy, and Research Lab Digitalization
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USD 140/hr
Executive certificate in Innovation management and entrepreneurship
Germany

I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...

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USD 140/hr
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Karthickeyan V.

2.3 years experience in Eumdr. As a part of MDR, I'm doing freelance work in writing CER and preparing EU Technical doc.
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USD 10/hr
BE
India

I'm an Engineering graduate having around 7 yrs experience with expert knowledge in EUMDR.

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USD 10/hr
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Mohan M.

Expert Freelance Consultant Standards, Regulatory Affairs & QMS for Medical Device Design & Manufacture
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USD 125/hr
M.E. (Control Systems)
India

Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...

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USD 125/hr
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Biomedical E.

MEDICAL DEVICE REGULATORY CONSULTANT EU-MDR | EU IVDR | SaMD | FDA | MHRA | SFDA | Germany | 7+ years’ Experience
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USD 30/hr
MS Biomedical Engineering
Pakistan

I am Umair Ahmed, a seasoned Biomedical Engineer and Scientist offering over 7 years of comprehensive experience in the freelance medical devic...

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USD 30/hr
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Hana A.

Regulatory affairs specialist with 8 years of experience in medical devices and pharma registration in ASEAN region.
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USD 50/hr
BSc in Biotechnology
Malaysia

Regulatory submission to Health Authority, GDPMD, QMS, ISO 13485, GDP, Post market surveillance and audits.

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USD 50/hr
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Pragatheeshwaran N.

Four plus years of hands-on working experience in Medical device PMS complaints handling, vigilance and RPA (Uipath )
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USD 20/hr
B.E
India

Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...

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USD 20/hr
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Haralabos P.

Medical/Pharma English into Greek translator with medical background (MD, MSc, PhD, Certified Radiologist)
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USD 35/hr
Certificate in Translation
Greece

Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...

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USD 35/hr
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Find European Medical Device Regulation (MDR) Experts for hire on Kolabtree. Get consulting services from experienced specialists. Hire an EU MDR consultant today.

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