IVDR (In Vitro Diagnostic Regulation) Specialist

The Turku Site, with over 500 employees, represents one of Revvity’s major manufacturing and product development sites for newborn, maternal fetal health, and prenatal screening. As the global market leader in newborn screening, our solutions have tested over 700 million babies worldwide for life-threatening diseases.

Now we are looking for candidates for the position IVDR (In Vitro Diagnostic Regulation) Specialist. It is a fix-term contract position to the end of March 2025.

Role description:  

• You will update product technical documentation to meet IVDR requirements.   

• You will collaborate with R&D, Regulatory Affairs, and Quality.

Role requirements:  

• Degree in Biochemistry, Biotechnology, Molecular Biology, Genetics, or similar.

• IVDR knowledge and/or experience from compiling technical documentation for medical device registrations.

• R&D background is appreciated.

• Fluent reporting and communication skills in English and Finnish   

• Proactive, resourceful, independent and a good team player in the cross-functional team.

What we offer:  

• Inspiring leadership and exceptional employees.

• Dynamic and innovative culture.

• Focus on career development.

• Collaborative and diverse environment.

Will you be our next top professional? Join us today – For the better!

Revvity Turku Site is a drug free site and a medical examination for new employees includes a drug test.