Descripción
RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Do you want to contribute to improving the care of cancer patients by helping ensure the quality and compliance of innovative software medical devices? Join RaySearch and become part of our Quality & Regulatory Affairs team. In this role, you will work closely with colleagues across the organization to support and continuously improve our Quality Management System, enabling the development and delivery of safe and effective products to patients around the world. About the role As a Quality Specialist, you will be part of a dedicated Quality & Regulatory Affairs team supporting a growing and innovative medical device organization. You will be involved in a variety of quality activities across the product lifecycle and have the opportunity to work closely with colleagues throughout the organization. The role focuses on maintaining and improving our Quality Management System while supporting the organization in meeting regulatory and quality requirements in a practical and efficient way. Your main responsibilities Support the maintenance and continuous improvement of the Quality Management System (QMS), related quality processes, and electronic QMS platforms. Manage and support CAPA, non-conformity, and change control activities. Plan, conduct, and follow up