Hire an ISO 13485 Consultant: Find ISO experts on Kolabtree

Dr. Alexandra A.

Medical Devices 💊| Biocompatibility 🧪| Sterilization 🧫 | Regulatory Affairs 📝 | Radiatio...
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USD 150/hr
PhD
Portugal

With 16 years of industry and academic experience combined in the medical device and interventional oncology fields, I am passionate about alig...

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USD 150/hr
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Dr. Somnath Swami V.

Scientific & Medical Writer | Research Consultant | Pharmaceutical Sciences Expert ...
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USD 9/hr
M. Pharmacy
India

Researcher with expertise in solubility enhancement and formulation development of pharmaceutical compounds, focusing on the use of mesoporous ...

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USD 9/hr
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Woodrow S.

Medical Device Quality & Regulatory Consultant; ISO xxxxxxxxxx, FDA, MDSAP, EU MDR Compliance
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USD 75/hr
Biomedical Engineering
United States

I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...

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USD 75/hr
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Yanka R.

MedTech Consultant | BioInnovate Fellow | Market, Clinical & Regulatory Insights
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USD 85/hr
MSc in Biomedical Device Materials
Ireland

I’m a biomedical innovation professional with a background in materials engineering, medical device development, and clinical translation. As a...

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USD 85/hr
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Dr. Diana K.

MD | MS in Bioinformatics & Data Science | Medical Writer & Clinical Project Manager in Pharma & MedTech
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USD 60/hr
Master of Engineering in Bioinformatics
Armenia

I’m a medical doctor (OB/GYN), bioinformatics & data science graduate, and experienced medical writer with 4+ years in clinical trial suppo...

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Dr. Jan S.

Scientfic Expert | Critical Reader and Writer | PK/PD Specialist | Experiment and Product Designer | Regulatory Affairs
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USD 60/hr
Doctor of Philosophy - PhD
Austria

🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...

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USD 60/hr
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Dr. Evrim Atılay T.

Freelance expert. 15+ pharma industry experience in R&D and regulation on regulated & non-regulated markets.
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USD 12/hr
PhD
Turkey

Throughout my career, I have led cross-functional teams in pharmaceutical development across leading companies in Turkey. I have successfully d...

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USD 12/hr
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Prafullakumar P.

Medical Device Regulatory Compliance Expert (ISO 13485, Risk management, EU MDR, MDSAP. US FDA).
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USD 20/hr
Masters of Science-Medical Device
India

I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...

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USD 20/hr
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Dr. Shifa J.

Regulatory Affairs and Scientific Research professional
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USD 30/hr
Graduate certificate
Canada

Regulatory Affairs and Scientific Research professional with 6+ years of combined experience in biotech, academia, and government. Skilled in r...

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USD 30/hr
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Kolabtree is the leading online marketplace for ISO 13485 consultants. Post your project, get bids, and hire an ISO 13485 expert.

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What Is an ISO 13485 Consultant?

An ISO 13485 consultant is a medical device expert who helps organizations meet specific quality management requirements, particularly in terms of fulfilling regulatory requirements related to medical device manufacturing, design, safety and market launch.

What Does an ISO 13485 Consultant Do?

An ISO 13485 consultant comes armed with deep knowledge on medical device quality management requirements, aligning these to what external parties such as certification bodies use for their judging and auditing purposes.

The expert’s recommendations help medical device companies ensure that their product meets these specific requirements across the supply chain, such as production, design and installation. This also extends to regulatory and compliance requirements, such as risk management and safety expectations.

Qualifications for an ISO 13485 Consultant

ISO 13485 experts typically have niche expertise and knowledge on the intricacies of medical device design certifications and process, as well as a working knowledge of how and when these requirements are updated. This involves,

  • Intense training and vast experience in manufacturing process systems
  • Auditing strategies and compliance knowledge and related certifications
  • Thorough understanding of quality management systems, risk management and medical device efficiency

Benefits of Hiring Freelance ISO 13485 Consultants

Considering quality management is a periodic requirement for medical device manufacturers, hiring an on-demand ISO 13485 consultant makes a lot of financial and strategic sense. 

These freelance experts are typically highly qualified, and possess past experience from high-impact projects. This also enables organizations to hire the best ISO 13485 expert irrespective of location, since freelance platforms have independent scientists and consultants registered across the globe.

Cost of Hiring an ISO 13485 Consultant

ISO 13485 consultants charge according to a wide range of factors, such as scope of the project, duration of the consultation required, and the market impact of the medical device in question.

Since niche factors such as safety, design and compliance are hard to define tangibly, consulting these experts on-demand can be a more feasible option throughout the supp[ly chain.

On Kolabtree, you can hire freelance ISO 13485 consultants for as low as $35/hour, with more experienced freelancers charging up to $200/hour.

How to Post a Project to Hire ISO 13485 Experts

Before posting a project, you need to decide the following criteria in terms of hiring a freelance ISO 13485 expert,

  • The particular quality management, medical device design or regulatory compliance process you’re hiring for
  • The skills and experience you want the ISO 13485 consultant to possess
  • The budget and duration of the project

Now, post a project on Kolabtree detailing these requirements step by step, which will ensure you receive quality proposals from the best independent ISO 13485 experts around the world. Alternatively, you can directly browse through the best experts available for consultation, and pick one that suits your requirements.