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Eurotrol's logo
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PT, INR, ACT and aPTT in one vial for all POC Coag instruments.
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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.
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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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Quick access to stay in the know about our newest products and improved services.
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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 Customer Service Teams in The Netherlands and US are available to assist with any questions or needs.
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Our searchable document library contains needed supporting documents for our products.
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Comprehensive learning and education tools for our products and their uses.
Product Development Documentation Specialist
Ede
The Netherlands
Product Development
Full-time
At Eurotrol, our Product Development Documentation Specialists play a vital role in driving innovation and ensuring excellence in our in vitro diagnostic (IVD) medical device offerings. As a Product Development Documentation Specialist, you will be responsible for managing documentation for new products and updates to existing ones, from planning through implementation. Your expertise will help shape the future of our R&D efforts and contribute to our global success.
We're looking for a proactive and detail-oriented professional with a strong background in IVD medical device documentation, project planning, and validation processes. If you thrive in a collaborative environment and are passionate about delivering high-quality results on time, we'd love to hear from you.
Key Responsibilities
- Plan and manage the documentation around medical device development projects and product changes
- Lead product verification and validation studies
- Perform software validation activities
- Coordinate design transfer with Process Development Engineers
- Lead cross-functional taskforces for product development
- Ensure timely progression through all development phases
- Communicate effectively with customers and internal stakeholders
Qualifications & Skills
- Proven experience in a similar role, preferably within the (IVD) medical device industry
- Bachelor's degree or higher (preferably in the field of life sciences)
- Strong project management and deadline-driven mindset
- Exceptional attention to detail and analytical thinking
- Effective problem-solving and decision-making skills
- Excellent verbal and written communication in English
- Team-oriented with a collaborative and positive attitude
- Quality-conscious and committed to continuous improvement
- Ability to foster a productive and communicative work environment