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

Diploma in Quality Auditing
Australia
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USD 150/hr

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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USD 150/hr

Vision-driven executive with over 21 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...

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USD 150/hr
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Master of Communication in Digital Media
Germany
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USD 50/hr

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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Master of Public Health
United States
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USD 50/hr

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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BEng Hons Manufacturing Engineering
United Kingdom
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USD 150/hr

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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Bachelor in Biomedicine
Brazil
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USD 80/hr

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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USD 150/hr

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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Master of Public Health
France
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USD 100/hr

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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Environmental Enineering - M.Sc
Ireland
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USD 200/hr

I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...

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USD 200/hr
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Masters of Pharmacy
India
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USD 45/hr

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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M.E. (Control Systems)
India
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USD 125/hr

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 Engineering
India
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USD 10/hr

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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USD 8/hr

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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USD 10/hr

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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USD 20/hr

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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USD 200/hr

30+ years experience in MedTech. NICE MedTech Early Technology Assessment (NICE MetaTOOL) facilitator. Proven record in getting great technolog...

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USD 200/hr
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M.Sc Biochemistry
India
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USD 100/hr

▪ Writing, reviewing quality and ensuring timely delivery of CEP/CER, PMSP/PMSR/PSUR to the client according to EU-MDR/MDD regulations and rela...

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USD 100/hr
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BSc in Biotechnology
Malaysia
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USD 50/hr

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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Consult top freelance European medical device regulatory (mdr) specialists with expertise in regulatory guidance, regulatory systems, and more. Kolabtree is the world's largest platform for hiring trusted freelance scientists and consultants.

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