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Top Freelance Medical Device Validation Experts for Hire

Sachin B.

Pharma GxP: AI Validation, CSV/CSA & Quality Transformation"
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USD 200/hr
MBA
Belgium

Senior Pharma Quality & Digital Transformation Leader 25+ years building GxP-compliant systems at scale across Boehringer Ingelheim, Sun Ph...

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USD 200/hr
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Ojas K.

End-to-end IVD consultant specializing in ISO 13485, CE-IVDR compliance, QMS, and diagnostic product development
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USD 40/hr
M.Sc. Microbiology
India

IVD regulatory and product development specialist with 10+ years of experience in diagnostic virology, immunoassay development (ELISA, rapid te...

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USD 40/hr
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Dr. Rupak D.

Materials Testing and Characterization Service (https://materialsmetric.com/)
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USD 175/hr
Ph.D in Biomedical Engineering with specialization in regenerative medicine
United States

Materials Metric specializes in advanced material testing and characterization, serving clients across industries including pharmaceuticals, ae...

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USD 175/hr
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Valentina L.

Biotechnologist & PhD Candidate in Biological Sciences | Molecular Biology, PCR & Scientific Writing
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USD 20/hr
Bachelor’s Degree in Biotechnology
Argentina

My undergraduate thesis focused on environmental remediation assays, where I worked on experimental design, sample analysis, and evaluation of ...

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USD 20/hr
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Rui D.

Ph.D. Biomedical & Veterinary Scientist | Regenerative Medicine Expert & Consultant
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USD 70/hr
PhD Student
Portugal

I am a PhD-level researcher, Assistant Professor, and Academic Coordinator with over a decade of experience spanning Veterinary Medicine, Regen...

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USD 70/hr
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José Daniel C.

Medical Device Regulatory Affairs & Market Access Specialist | LATAM Health Policy
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USD 60/hr
Masters of Public Health
Colombia

Biomedical Engineer, Microbiologist, and Master of Public Health (MPH) with over 5 yea...experience in the global medical device industry and healthcare public affairs....

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USD 60/hr
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Dr. Robbie C.

Computational neuroscientist with virtual healthcare industry experience.
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USD 150/hr
PhD | Neuroscience
United States

AI/ML Engineer and Data Scientist with a decade of experience driving digital health innovation from startup inception to large-scale data solu...

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USD 150/hr
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Dr. Adam S.

PhD Academic Writer | Dissertations | Thesis | Research Papers | Researcher | Scientific Writer | Editor | Proofreader
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USD 8/hr
Doctor of Education (EdD)
India

Former university professor & PhD-qualified academic consultant with 12 years of experience delivering publication-ready dissertations, the...

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USD 8/hr
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Jarrell M.

Medical Device Consultant | Risk & Regulatory Compliance | ISO 14971, IEC 60601, ISO 13485, FDA 510(k), EU MDR
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USD 150/hr
Bachelor of Science in Electrical Engineering
United States

I am a medical device consultant with 25 years of experience helping companies bring products to market. I combine strong expertise in regulato...

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USD 150/hr
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Thomas M.

Scientific Consultant | Cognitive & Computational Neuroscience | CNS Drug Delivery | Data Analysis
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USD 175/hr
PhD, Computational Neuroscience
United States

PhD Research Scientist; Expertise in neuroimaging, brain science, CNS drug delivery devices, computational approaches including machine learnin...

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USD 175/hr
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Andrei L.

Medical AI Solutions Architect | EU AI Act & MDR Compliance Expert | Custom RAG & Python Developer
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USD 100/hr
Engineering in Biotechnology
Romania

I bridge the gap between clinical requirements and advanced AI architecture. With a strong background in Healthcare & Medicine and deep tec...

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USD 100/hr
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Dr. Florence L.

Medical Device & IVD Regulatory Affairs and QMS Advisor | MDR, IVDR, UKCA, FDA (60 minutes consultation)
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USD 120/hr
PhD
United Kingdom

Medical Device and In-Vitro Diagnostics Regulatory Affairs and Quality Assurance (QARA) professional with 6+ years’ experience supporting medic...

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USD 120/hr
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Kay G.

Freelance (Bio)Pharma industry consultant/contractor (Expert Regulatory, Quality & Compliance - 30+ years experience...
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USD 72/hr
MBA
Canada

Industry consultant/contractor with extensive hands-on experience assisting offshore and domestic clients in bringing molecules to market. Sub...

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USD 72/hr
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Dr. Seval K.

Global Life Science Advisor – Quality Assurance & Controls - Regulatory Affairs - R&D - Production - Clinical Af...
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USD 280/hr
Chemistry PhD
Turkey

Quality Assurance , Validation Planning and Reporting , Medical Device Clinical Study Design and Reporting by CER PSUR and else. , FDA Register...

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USD 280/hr
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Dr. Abdullah O.

Innocentive solver ( 4 awards), Prof of Biochemistry and Clin. Biochem, Biogerontologist, Bioinformatician, 30+y exp, MD
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USD 95/hr
Master of Bioinformatics
United States

I seek opportunities where I can leverage my expertise in aging biology (biogerontology), biochemistry, clinical biochemistry, bioinformatics, ...

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USD 95/hr
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Ashley K.

Medical Device Regulatory Affairs & QA Specialist | EU IVDR, ISO 13485, CAPA, Post-Market Surveillance
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USD 60/hr
Bachelor of Science in Biology
United States

Regulatory Affairs and Quality Assurance specialist with nearly three years of hands-on experience supporting medical device and IVD manufactur...

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USD 60/hr
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Oskar S.

EU MDR Regulatory Affairs Consultant — Clinical Evaluation, Literature Reviews & Technical Documentation
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USD 75/hr
MSc Biomedical Engineering
Czech Republic

Regulatory affairs specialist with hands-on experience taking medical device manufacturers through the EU MDR transition. In my Quality & R...

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USD 75/hr
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Kolabtree is the leading online freelance marketplace for Medical Device Validation experts. Post your project, get bids, and hire qualified experts quickly and easily.

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Kolabtree ensures the safety and security of your payments, personal information and project details. Kolabtree’s T&C include a default confidentiality and NDA clause.

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You can choose to pay either a fixed or an hourly fee based on your scope of work. Pre-pay for the next milestone. You have to approve the deliverables only if the quality meets your expectations. If you aren't happy, we'll refund your money.

Kolabtree will share multiple quotations for your project. You have the freedom to accept the quote that aligns with your project requirement and budget. You can get in touch with us if you want to discuss the fee.

Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.

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Job Done!

Approve the deliverables once you're satisfied with the job done.