Trainee, Quality and Regulatory Affairs

Nexstim is a Finnish growth-oriented medical technology company. Our transcranial magnetic stimulation (TMS) systems have the essential approvals to market and sell in for example Europe and North America. We operate under ISO 13485, MDR, and FDA QSR, product quality as our priority as we make our state-of-the-art technology available to patients as widely as possible. 

The position of a Trainee, Quality and Regulatory Affairs is part-time (2-3 days per week or as agreed). The employment is temporary until the end of the year or as agreed. This job requires attendance at our office in Vallila, Helsinki, with the possibility for occasional remote work. 

Typical tasks include:

• Assisting collection and creation of regulatory and technical documentation during the product development projects of medical devices
• Supporting collection, creation and updating of regulatory submissions and sales licences
• Improving and updating Nexstim’s quality management system according to global standards and regulations

We appreciate:

• Final stage studies or a degree in applicable technical field (for example medical device technology)
• Fluent communication skills in English and Finnish   
  • In addition to processing documents in both English and Finnish, fluency in both languages is needed for reading and interpreting laws and documents
• Interest in medical device technology and regulation
• Any work experience from a medical device company 

To apply for this post, please send your CV and an application letter in English to: rekry@nexstim.com by January 31, 2025. For more information on the position, please contact Anneka Kruuti, Quality & Regulatory Affairs Specialist at anneka.kruuti(at)nexstim.com.