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Medical Device Compliance Expert
2 weeks ago
Cancer patients deserve the best possible treatment options.
Position OverviewThis 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
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 OfferAs 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.