(Poistunut julkaisusta)

RA Specialist
Radiometer Turku Oy

Alkuperäinen julkaisupäivä 11.9.2018


Regulatory Engineering Partner

Imagine opening a box full of technologically advanced medical devices designed to help caregivers make diagnostic decisions that save lives. You immediately feel the curiosity to learn more about the functions, designs and ideas behind these inventions. Now you can open that box and begin a professional journey in Radiometer Medical, a successful medical device company. This job is your opportunity to impact regulatory aspects and compliance related to the development and product life cycle of several medical devices. 

Combine your engineering background with quality mind-set

Your future colleagues, many of who has been in Radiometer for several years, look forward to work with you because you are passionate and persistent. We need your ability to deliver quality on time and your attitude that ensures that what you don’t know today, you will learn tomorrow.

We are expanding our activities at Radiometer Turku and therefore, you have the chance to quench your thirst for knowledge by applying for this role and learn all about how we combine complex technology consisting of software, hardware, electronics, chemistry and mechanics for important usage in the healthcare industry. You will be joining the RA Immunoassay team that consists of one specialist in Turku, 4 specialists and a manager in Denmark.

Your assignments

You might not have previous experience with all of the following assignments, but your engineering or science background combined with curiosity about development of medical devices enables you to work with:

  • Support to cross-functional research, and regulatory projects
  • Interpret legislation and ensure implementation
  • Participate in process improvements and creation of SOPs in the RA area
  • Support regulatory compliance in change control process

We value experience in the following areas:

  • A Master's Degree/ student Ph.D. in Science, Biochemistry or the like.
  • Medical device legislation (IVDD, MDD) on different markets
  • RA support to cross-functional projects
  • A proven track record of compiling regulatory files and achieving approvals worldwide
  • Fluency in English, both written and spoken.
  • Experienced MS Office, working with databases and Adobe Acrobat Pro

You must be passionate and committed about what you do, as well as:

  • Using your analytical skills and sound judgment to make fact-based decisions
  • Able to work with transparency and build trust to working partners
  • Be positive and open-minded, adding energy to the team by taking responsibility.
  • Have strong communication skills, communicating effectively across teams, functions, and cultures.
  • Focused on targets and results, acting proactively and working well independently as well as in teams.
  • A can-do attitude with the ability to handle and prioritize many projects at the same time.

For further information, please contact Nina Christensen by phone + 45 4048 8418, best available on 14.9.2018 at 10.30-12.30 or on 20.9.2018 at 11.00-13.00 or by e-mail at nina.christensen@radiometer.dk.

Please submit your application, resume and your salary request to info@radiometer.fi by September, 26th 2018.