Hire Medical Device Freelancer: Find Medical Device Engineering Consultants

Viktoria K.

Idependent Clinical Study Protocol Reviewer and Specialist with 14 years in depth experience in clinical research| Coach
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USD 200/hr
Environmental Enineering - M.Sc
Ireland

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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Tamil S.

5 years experience as an Quality Assurance professional.
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USD 60/hr
Bachelors of Engineering
India

5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...

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USD 60/hr
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Minh Tuan T.

High-achieving individual with 4+ years in medical device regulations (EUMDR & FDA) and business process development...
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USD 85/hr
Masters of Science
United States

Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...

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USD 85/hr
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Veer P.

IVD Regulatory Affairs Expert | Experience in Technical Documentation Writing for IVDR CE Projects
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USD 30/hr
Master of Pharmacy (M.Pharm) in Pharmaceutical Regulatory Affairs
India

A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...

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USD 30/hr
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F H C.

Medical Research and Development, with patient-oriented readiness.
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USD 79/hr
Environmental Engineering
Netherlands

I offer support for: Regulatory Affairs Clinical Trials and Trial Management Evidence-Based Medicines and Outcomes Research Non-clinical Develo...

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USD 79/hr
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Deepa G.

Expert in Medical Writing/ Regulatory Affairs consultant
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USD 70/hr
Master of Business Information Systems
Netherlands

➢Medical writing as per new regulation -Clinical (CEP, CER, Literature review, PMS plan etc) & Non-clinical documents (DOC, Risk Analys...

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USD 70/hr
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Jenny V.

Freelance Specialist Medical, Health and Technical Writer
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USD 75/hr
Diploma in Applied Science (Sonography)
Australia

My background is nearly two decades in a clinical environment in medical imaging spread over the UK, New Zealand, Australia, and Timor Leste. ...

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USD 75/hr
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Megha B.

Health Economics, Market Access, Systematic Literature Review, Meta analysis (15+ years experience)
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USD 100/hr
Economics
United States

I have 15+ years of experience in health economics and outcomes research (HEOR) and market access in the US and globally. I have prepared healt...

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USD 100/hr
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Rakesh S.

Exp in Medical Device Packaging,Clean room Operations,Sterilizationand Medical device process Validation
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USD 50/hr
Masters of Science
India

Specialized Focus Areas: • Standards and Regulations of Medical Device ISO 13485 and 21 CFR part 82 • Sealing process characterization study ba...

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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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Alexey D.

Manufacturing Consultant Product Development - Medical Device 15+ years of experience in manufacturing engineering
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USD 95/hr
Masters of Science - Material Science
Canada

Product Design - ​Design based on expertise from the manufacturing environment, we support engineering teams by providing guidance on best prac...

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USD 95/hr
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Tara N.

Biomedical writer experienced in research regulatory evidence-based writing/editing. AMWA member. 5+ years,
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USD 75/hr
Masters
United States

Masters in Biomedical Sciences, biotech, pharma experience. ICH CORE AMA MEDDEV FDA. Scientific writing/editing, research regulatory CME

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USD 75/hr
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Rayan T.

Scientific Researcher | Academic Writer | Digital Health | Mental Health | Digital Mental Health
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USD 50/hr
United Kingdom

👩‍💼 I am a published scientific researcher. I currently work in academia at King's College London. My areas of expertise ar...

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USD 50/hr
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Rob F.

Quality System and Regulatory professional with over 20 years of experience
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USD 75/hr
Bachelor of Science in Applied Arts and Sciences Biology
United States

Rob is a Quality System and Regulatory professional with over 20 years of experience in QMS development, deployment, and remediation in the med...

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USD 75/hr
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Ellen S.

Writer & Scientific Consultant: Biotech | Psychology | Project Management | Digital Marketing | Scientific Research
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USD 65/hr
Master of Arts (M.A.)
United States

A dedicated and driven professional with a diverse background in biotech and a strong foundation in project management and scientific consultin...

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USD 65/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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Mawaddi Q.

Clinical Evaluation Specialist | Audiologist |
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USD 40/hr
Master of Medical Sciences (Audiology Sciences)
Malaysia

A clinical Evaluation specialist with clinical, research and occupational audiology background. I'm passionate in clinical research and any...

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USD 40/hr
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João M.

Medical devices; polymers; elastomers; Data Management and visualization; surgical adhesive; 3D printing
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USD 100/hr
PhD
Portugal

I’m a biochemist specialized in materials science; I have over 15 years experience in a mixed context of academic and industrial environments, ...

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USD 100/hr
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Nicole R.

Expert Project Manager Consultant in Clinical Research
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USD 80/hr
Bachelor of Arts
United States

Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...

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USD 80/hr
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Prerana D.

Clinical research professional having an extensive knowledge on medical devices CE marking and consulting services.
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USD 10/hr
M.Sc Clinical Research
India

A clinical research post-graduate having a vast knowledge over a range of Medical devices consulting services on conformation of 62304:2006 sta...

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USD 10/hr
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Rukmani S.

Freelance science writer/editor
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USD 60/hr
PhD
India

I am a biomedical research scientist and a science communicator based in Ireland with over 8 years experience writing/editing manuscripts, prep...

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USD 60/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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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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Asma S.

Medical content writer with 7+ diverse experience in intellectual property research analysis and medico marketing
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USD 8/hr
Master in Pharmacy
India

A dynamic result-oriented professional holding a noteworthy 7+ years of diversified experience in the area of Intellectual property analysis an...

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USD 8/hr
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Boris L.

Registered US Patent Agent, Inventor, Entrepreneur - medical devices and more
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USD 150/hr
MS Mechanical Engineering
United States

I prepare and prosecute patent applications with the USPTO and internationally

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USD 150/hr
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Hire medical device consultants for help with FDA approvals, 510(k) submissions, EU MDR compliance and more. Get end-to-end product development support. Work with medical device engineering consulting experts for help with content writing and medical copywriting.

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Recent Projects
  • Hire medical device freelancer for FDA approval
    $500.00
  • hire medical device engineering consultants for EU MDR
    $400.00
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What Does a Medical Device Engineering Consultant Do?

A medical device consultant works with medtech companies to help them develop and design products, meet regulatory requirements, conduct clinical trials and market the product. A medical device expert can have 10-20 years of experience in the field in the areas of compliance and product design. A medical device writer can help with regulatory documents such as FDA submissions, Clinical Evaluation Reports, clinical trial protocols, and grants, as well as with content writing requirements such as white papers, blog articles and press releases. Companies worldwide are increasingly seeking medical device expertise on demand as it allows the flexibility of hiring remote workers as and when required. 

Why Approach Experts Instead of a Medical Device Consultancy?

Medical device companies have typically used a medical device consultancy to outsource their tasks. However the freelance revolution has made it possible for them to hire experts for short-term or contract projects. Hiring experts directly requires no minimum commitment or contract. A medical device engineering consultant freelancer can provide a variety of services ranging from literature search and systematic reviews to statistical analysis and clinical research. On Kolabtree, it's quick and easy to directly contact a freelancer and have one-to-one conversations about your requirements. 

How Medical Device Writing Experts Can Help

A medical device writing expert can provide a wide range of services that help medtech SMBs save precious time and energy. These include but are not limited to:

  • Developing 510(k) submissions for FDA approval
  • Developing CERs, clinical research protocols, and clinical case studies
  • Putting together grant applications and proposals
  • Writing and reviewing blog articles, website content, white papers and ebooks
  • Writing and editing research papers and preparing them for journal publication

Working with a medical device writing consultant is becoming an increasingly popular choice among medtech businesses so that they can streamline their resources. With scientists and industry experts working remotely, it's possible to access medical device expertise in domains like cardiology, orthopedics, medical imaging, and more. 

As a Medical Device Company, What Functions Can You Outsource?

From ideation to product marketing, medical device engineering consultants can work with you at every stage of the product cycle. A medical equipment consultant can improve and optimize the design of equipment such as MRIs, ultrasound machines, etc. Biomedical engineers can work on a contract basis to provide prototypes and the final product design. A medical device marketing freelancer can develop creative campaigns and brand messaging to position your product in the market. A medical device development freelancer is typically an experienced expert, who can help with validation, verification, testing and compliance of the product. Medical writing is one major function that can easily be outsourced to qualified experts: a medical device writing freelancer can develop compelling, authoritative copy for your target audience.  

How Much Does It Cost to Hire Medical Device Experts?

The hourly rate for hiring medical writers on Kolabtree is $40 to $70. The fee for your project will depend on the expertise required, how urgently the work is needed, and what level of speciality you're looking for. Medical device consultants who work on design, development and compliance can charge up to $300 per hour. On Kolabtree, you can discuss your requirements directly with experts and get a range of quotes before choosing the best expert based on your budget and timeline. 

Hire Medical Device Engineers by posting a project for free.