Editor / Medical Writer

MAIN PURPOSE OF THE JOB

The Editor plays a crucial role in ensuring the accuracy, clarity, and compliance of all written materials produced by our company. This position is essential for maintaining our commitment to providing high-quality and compliant documentation that is required in the highly regulated in-vitro diagnostic (IVD) medical device industry in which Eurotrol operates.

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KEY RESPONSIBILITIES

As an Editor, your responsibilities encompass:

• Editing and Proofreading: Review and edit a wide range of documents, including regulatory submissions, standard operating procedures, work instructions, forms, templates, training materials, protocols and reports for grammatical, typographical, and content accuracy.
• Compliance: Ensure that all documentation complies with relevant regulatory standards, such as FDA guidelines and ISO requirements.
• Consistency: Maintain consistency in style, tone, and terminology throughout the company's documentation.
• Clarity: Simplify complex medical and technical content to make it understandable to a diverse audience, including production personnel, healthcare professionals, regulatory bodies, and end-users.
• Collaboration: Work closely with subject matter experts, and other stakeholders to gather accurate information and provide feedback on content, actively participating in project teams as needed.
• Document Review: Participate in document review processes, ensuring all documents undergo rigorous scrutiny for accuracy, clarity, and compliance before publication or submission.

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REQUIRED EXPERIENCE & SKILLS

• Bachelor's degree (or higher) in technical writing, business, or a related technical field.
• 1-3 years of experience in technical writing.
• Proficiency in the Microsoft Office suite, with a focus on Word and Excel.
• The ability to work both effectively as part of a project team and independently on tasks.
• Capacity to understand engineering and other technical information.
• Prior experience in the medical device industry is a plus.

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THE COMPANY

Eurotrol, operating under the "CueSee" brand, specializes in developing, producing, and distributing quality controls for in-vitro diagnostic (IVD) medical devices used globally. Our customers include medical device manufacturers, hospital laboratories, OEM diagnostics companies, and external quality control organizations.

Since our establishment in 1988, we have become a leading player in the field of quality controls for IVD medical devices. Our portfolio comprises over 400 products covering a wide range of tests that are distributed in more than 80 countries. Our company has a total of 60 employees and is located both in the Netherlands and the USA. Its headquarters is based in Ede, the Netherlands, where Production and Research & Development takes place in accordance with “ISO 13485 - Medical Devices”. In Elizabethtown, KY, USA, we operate a subsidiary dedicated to product distribution and sales support, serving both the USA and the broader North and South American regions. The official company language is English.

We prioritize investing in our employees to support their personal growth and maintain a professional and pleasant working environment. Eurotrol is a privately owned company with an innovative and entrepreneurial culture, characterized by short communication lines. We encourage employees to take initiative and participate in projects across the organization. These attributes have enabled us to develop a series of unique breakthrough products, which are now being introduced to the market, driving substantial business growth in the years ahead.

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OUR OFFER

• A position in a healthy organization with a promising future
• Personal development through guidance, education and knowledge sharing
• A competency development model focused on your personal ambitions
• Support in creating a safer healthcare
• Able to leave your mark on the job
• A market-competitive salary and dynamic work environment