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Medical Device Compliance Expert

2 weeks ago


Stockholm, Stockholm, Sweden TN Sweden Full time

Cancer patients deserve the best possible treatment options.

Position Overview

This QA/RA Specialist role is a unique opportunity to contribute to the development of innovative software solutions for cancer care.

Key Responsibilities
  • Manage the transition of our Quality Management System (QMS) to a new digital platform
  • Lead the Corrective Action Preventative Action (CAPA) process and train colleagues on individual CAPA management
  • Collaborate with our Information Technology (IT) department to validate tools supporting the QMS
  • Support internal audits, external audits, and inspections
Requirements

To succeed in this role, you should have previous experience with QMS maintenance, project management, and excellent communication skills. A strong understanding of medical device regulations and quality management systems is essential.

What We Offer

As a member of our team, you will have access to ongoing training and development opportunities, as well as a dynamic and inclusive work environment that encourages collaboration and innovation.