(Poistunut julkaisusta)

Regulatory Specialist
KaVo Kerr Group Finland

Alkuperäinen julkaisupäivä 2.11.2018

We are now looking for a

Regulatory Specialist

to support our global product registrations. The role is responsible for CE marking (MDD/MDR) and change notifications to our Notified Body as well as management of country specific regulatory holds in our ERP system. Together with the Regulatory Affairs team you will develop and maintain regulatory processes and tools, and attend regulatory audits as necessary.

We expect you to

  • hold an Engineering, Business or equivalent degree
  • have knowledge or great willingness to learn EU MDD/MDR and country specific regulatory requirements
  • have fluent communication skills both in Finnish as well as in English

As a person, you are self-motivated and able to work independently, yet an efficient team player, who strives for reaching the goals. You take initiative, learn quickly and enjoy facing challenges and solving problems. You have a sense of urgency and great attention to detail. You also enjoy working in an international company and multicultural environment.

We offer you inspiring challenges in a rapidly growing global healthtech business and an opportunity to work within a strong Lean culture. The position offers interesting and varying responsibilities and an attractive opportunity to excel your professional expertise.

This is a fixed-term position for a parental leave substitute from December 2018 to August 2019.

Please submit your application with a salary expectation and your CV by November 18h, 2018 via our online recruitment system at https://www.kavokerr.com/fi-fi/toeihin-meille. We are constantly going through new applications and the candidates with most compatible profiles will be invited to the next step of the recruitment process already during the application period, so if you want to join us act now!



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