Validation Documentation Specialist

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Radiometer, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We’re a team that celebrates diverse ideas and continuous improvement. Here, you’ll find a place to grow and make a real impact, with your unique perspective driving us forward in improving patient care. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

Learn about the Danaher Business System which makes everything possible.

The Validation Associate is responsible for writing and maintaining validation documentation for software and electronics in NPI.

This position reports to the Senior manager and is part of the Manufacturing Development department located in Brønshøj and will be an on-site role.

This is a temporary position to cover a maternity leave, with a duration of up to 8 months.

In this role, you will have the opportunity to:

• Create, update, and manage validation documentation for software and electronics.
• Collaborate closely with the engineering team, production and the IVDR project to gather necessary information and ensure accurate documentation.
• Facilitate effective communication and maintain a strong working relationship with QA to ensure alignment on validation standards and practices.
• Ensure that all documentation meets regulatory standards

The essential requirements of the job include:

• Bachelor’s degree in Engineering, or related education or experience.
• The ability to write clear, accurate and concise technical protocols and reports
• Good communication and interpersonal skills to effectively collaborate with multiple teams.
• Proficiency in written and spoken English
• Proficiency in Microsoft Office Suite

It would be a plus if you also possess previous experience in:

• Regulatory standards, compliance and validation documentation
• Working with manufacturing, software and medical devices.

Application

We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.

We look forward to seeing your application.

We thank you for your interest. Please read our Applicant Data Privacy Notice carefully here.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Placering
Bronshoj, Denmark, state: , cityCountry: Bronshoj, Denmark