Hire an ISO 13485 Consultant: Find ISO experts on Kolabtree

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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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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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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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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Ninja P.

Regulatory Affairs Professional (Medical Device Consultant)
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USD 39/hr
Regulatory Affairs Medical Device
Canada

An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...

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USD 39/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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Khalaf A.

QA Director & Regulatory Expert | GMP & ISO | Chemical Analysis & Process Optimization for Medical Devices |...
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USD 40/hr
BA, Chemistry
Saudi Arabia

With a Bachelor of Science in Chemistry from King Saud University and a proven tenure as a Quality Director at Advance Medical Company, I posse...

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USD 40/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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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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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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Albert S.

ISO 9001 & ISO 13485, Data entry,
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BSc
India

I have Experience in ISO 13485, ISO 9001, Quality management system, MDF preparation under the MDR rule 2017

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Laura F.

Commercial Enablement Leader | Strategic Market Analyst | Expert Launching HighSpot
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USD 190/hr
Bachelors
United States

Results-driven commercial enablement leader with 20 years of healtcare-related experience in marketing, sales, training and product management....

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USD 190/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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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.