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Quality Assurance Specialist Manufacturing

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Varian is the world’s largest manufacturer of medical devices and software for treating cancer and other medical conditions with radiotherapy, radiosurgery, proton therapy and brachytherapy. Our vision is a world without fear of cancer. To meet this challenge, we equip the world with new tools for fighting cancer.

 

At our R&D site in Dättwil, Switzerland, with more than 250 employees, mostly engineers, computer scientists and physicists we specialize in the development of imaging software and hardware as well as treatment management systems for radiation therapy cancer treatment. Bring your talent to a place where your work will help fight cancer. Join Varian’s Oncology Systems team, and the work you do can make a difference by helping to create a world without fear of cancer.

Quality Assurance Specialist Manufacturing

As a Quality Assurance Specialist Manufacturing at Varian, you are accountable that the production processes are documented, and specific controls are in place to ensure adequate quality at all production stages. You keep abreast of regulatory procedures and changes, and interact with our suppliers to ensure compliance throughout the complete supply chain.

You work in close collaboration with other teams and stakeholders in Europe and overseas. Finally, due to the safety critical nature of radiation therapy, your commitment to quality is a must.

 

 

Specific Responsibilities

  • Develop, evaluate, revise, and applie quality assurance methods for existing and new production tasks, and approves final product quality acceptance
  • Support, evaluate, and monitor that the required validations during the manufacturing process is performed, documented, and maintained
  • Is involved in design and development phase from beginning to streamline quality controls and the required production tools to the final production stage
  • Review of the manufacturing documentation for adequacy and ensures that they are consistent with the company wide, global processes

 

 

Desired Qualifications

  • Degree in engineering or related technical field with comparable educational background
  • Experience in manufacturing quality assurance and working with regulations applicable to medical devices
  • Experience of working and communicating with different regulatory authorities and corresponding relationships
  • Fluence in German and English, written and verbal

 

You are analytical, communicative and focused. You work structured and have an eye for details. In addition, you can express your ideas and research in written form. You are used to working independently, open to discussing ideas and solutions with your colleagues. You thrive in an international work environment and in cultivating your contacts with partners in Europe and overseas.

 

Have we sparked your interest in a challenging and exciting position in a global environment with a potential for development? We look forward to receiving your application and CV. Job Code 15917BR. APPLY HERE

 

www.varian.com/ch/daettwil

Baden / Steinhausen / Villigen / Steinhausen (ZG)

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