Revvity is seeking a Regulatory Affairs professional at our Turku site in Finland. The role involves planning and executing regulatory project activities, including the preparation and review of global IVD device documentation for international agencies.

The ideal candidate will have a B.Sc. or M.Sc. in biochemistry or biotechnology, a minimum of 2 years in a regulatory administrative role, and fluency in both Finnish and English. Join a committed organization that values skill development and diversity.