Regulatory Assistant/specialist

Revvity | About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we're able to push boundaries in pursuit of better human health.

Find your future at Revvity.

Revvity is currently looking for a

Regulatory Assistant/Specialist

Fixed term (6 months)

Turku, Finland / Regulatory Affairs

Our Turku site, Wallac Oy, is one of the largest production and product development units within Revvity's diagnostics business. Currently, more than 500 employees work in Turku. We develop and manufacture instruments, chemical reagents, and software for screening and research purposes. We are a market leader in providing screening systems for newborns and pregnant women, and our products are in use in over 100 countries.

Role Description:

Plan and execute regulatory project activities, including preparation, collection, and review of global IVD device registration documentation packages for international agencies/authorities worldwide

Support cross-functional activities within projects

Contribute to process improvements within Regulatory Affairs; recommend changes to company procedures in response to changes in regulations or standards

Provide general and administrative support to the Regulatory Affairs team

Role Requirements:

B.Sc. or M.Sc. or equivalent in biochemistry or biotechnology

Minimum of 2 years of experience in an administrative role, preferably within a regulatory environment

Basic understanding of IVDR and international IVD regulations

Familiarity with SAP and Documentum

Excellent organizational and communication skills

Ability to multitask, with a proactive approach and strong follow-through

Fluency in Finnish and English (both spoken and written)

We Offer:

Opportu