Then come and join our global team as Design Quality Assurance Specialist Varian (f/m/d) , to ensure the highest quality with a focus on R&D in the global Varian radiotherapy portfolio.

This position is full-time or part-time with a minimum of 30h/week.

Your tasks and responsibilities:

• You ensure compliance requirements according to applicable regulations, directives and standards, including 21CFR part 820 - QMSR, EU MDR regulation 2017/745, ISO 13485, and the company quality guidelines
• You ensure in close collaboration with design and engineering teams that all product realization processes are applied, and the product is quality-compliant
• One of your tasks is to review the design and development documentation for adequacy and ensure that they are consistent with the company wide, global processes
• You support, evaluate, and monitor the performance of required verification and validation processes and their documentation
• As Design Quality Assurance Specialist, you are involved in the design and development phase from beginning to support risk management implementing the required controls at the final production stage
• You define and ensure that statistical data is collected, and you analyze the statistical data thereafter
• You support the engineering teams with root cause analysis and corrective actions implementation

To find out more about the specific business, have a look at https://www.siemens-healthineers.com/products-services ; Varian

Your qualifications and experience:

• You hold a degree in engineering or a related technical field
• You have many years of working experience in product development
• Ideally, you have experience in quality management including international standards and government regulations applicable to medical devices or in another regulated industry
• Experience in areas such as artificial intelligence, cloud computing, cybersecurity, radiation‑emitting devices, or wireless communication is a Plus
• Ideally, you gained experience in design quality assurance in medical devices or in another regulated industry

Your attributes and skills:

• You have fluent English skills, both written and spoken. Good German skills are a Plus
• You know what is important in leadership communication and have mastered the claviature of internal communication
• Quality is close to your heart, and you like to implement our high standards together in the team when making sound risk management decisions
• In your role, your analytical skills and ability to work under pressure will help you with time-critical issues