Scope

The company is a leading provider of particle accelerator technology for cancer diagnosis and treatment, as well as industrial applications. Its proton therapy systems are used in leading cancer centers worldwide to deliver precise and accurate treatment, minimizing damage to healthy tissue. They also remain a large market leader in industrial particle accelerators for sterilizing medical devices and food.

This company is a great place to work if you are passionate about patient care, innovation, and cancer treatment. They are at the forefront for radiotherapy treatment globally, as such, this company could be a great platform in which to launch your career in the oncology industry. If you wish to join this medical device organization don’t hesitate to contact.

Responsibilities

• Ensure that products meet all global regulations, including approvals and registration requirements
• Formulate and maintain documentation and approval dossiers to support product approvals.
• Help development teams comply with all relevant regulatory standards.
• Provide quality support to engineering and service teams.
• Help to improve products and processes within the product line.
• Maintain and improve the quality management system.

About You

• 3 years’ experience in Quality and Regulatory work in the medical device industry (history with an area of radiotherapy would be ideal)
• Commutable distance Nuremberg (hybrid work is available)
• Masters in a scientific/technical sector
• Active team player in projects and can communicate effectively to others
• Fluent in German and English
• Experience with medical software