Regulatory Affairs Coordinator

5 days ago


Stockholm, Stockholm, Sweden RaySearch Laboratories AB (publ) - Stockholm Full time
About the Role

As one of our QA/RA Specialists, you will join a team of ten dedicated coworkers. The role requires previous experience from maintenance of Quality Management Systems (QMS), including document management, CAPA management and change management.

The QA/RA team is central to the company's business as it is responsible not only for the QMS but also for product market clearances, vigilance and internal and external audits. Since the pandemic, the team has grown from seven to eleven members and is expected to continue to grow.

Your Profile

To be successful in this role, you work in a very structured and meticulous way. You have an interest in QMS related tasks (e.g. document management, CAPA management, change management and tool validation) and experience from project management.

You adapt to changing conditions and have good communication skills. It is essential that you are well-organized but can be flexible when required. You recognize the importance of written processes and instructions and take initiatives to fill in any missing pieces.

Our Culture

Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer.

We take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care.



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