Document Editor/Quality Engineer Medical Devices

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• PT, INR, ACT and aPTT in one vial for all POC Coag instruments.

• Eurotrol has been trusted by customers worldwide to design, manufacture, and distribute custom-made quality control solutions for In Vitro Diagnostics (IVD), with over 400 unique products developed for use in more than 80 countries. We welcome new requests for tailored solutions that give our partners a competitive edge and help improve patient care.

• Founded in 1988 by Professor Dr. , a pioneer in clinical chemistry, Eurotrol was built on innovative ideas to create quality control materials for In Vitro Diagnostic (IVD) tests. Today as an independent company operating in Europe and the USA, Eurotrol produces high-quality control and validation liquids samples that help ensure clinical laboratories deliver reliable test results with distribution and use in over 80 countries.

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• Ready to join a growing company making a difference in healthcare? Want to be part of a company that values their motivated and dedicated staff as one of their biggest assets? Take a look at our open positions.

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• Our searchable document library contains needed supporting documents for our products.

• Comprehensive learning and education tools for our products and their uses.

Document Editor/Quality Engineer Medical Devices

Ede

The Netherlands

Process Development

Full-time

About the Role

At Eurotrol, quality is at the heart of everything we do. As our Document Editor / Quality Engineer , you'll be a key player in ensuring our Quality Management System (QMS) documentation meets the highest standards of clarity, accuracy, and compliance. Your work will directly support our mission to deliver reliable and innovative quality controls for in-vitro diagnostic (IVD) medical devices used in hospitals and laboratories worldwide.

You'll have a central position in our Process Development team and collaborate closely with cross-functional teams - process development engineers, project managers, production team leaders - to create and maintain documentation that drives operational excellence and regulatory compliance.

What you'll do

• Edit and refine documentation such as work instructions, manufacturing forms, project plans, risk studies, quality agreements, and specifications
• Ensure all documentation complies with Eurotrol's QMS and regulatory requirements. This includes performing: impact assessments, document content check, revision history description, check template requirements, error corrections
• Facilitate and participate in process and product risk studies (eg FMEAs)

What you bring

• Good writing and editing skills in English
• Bachelor's degree or equivalent
• 1-3 years comparable work experience
• Ability to work independently and collaboratively in a dynamic environment

What we offer

• A competitive salary package
• A professional, friendly, and supportive work environment
• Opportunities for personal and professional growth
• The chance to contribute to products that make a global impact in healthcare