System Verification Engineer

Remote - Switzerland
23.10.2019 | Position with re­spon­si­bil­i­ties | 100%

System Verification Engineer

When you join Varian, you’re joining an organization with nearly $3 billion in annual revenue, and more than 6,500 team members across more than 30 countries. You’ll be backed by a culture that is centered on fostering your creative potential, and experience the full support of an organization and leadership committed to inspiring you to do your best work. 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. We develop and manufacture products and solutions that innovate, support and streamline cancer-fighting solutions worldwide. Our teams have a common drive to help others, and a passion for excellence. Join Varian and add your talent to the fight against cancer.

At Varian, our culture is centered on fostering the creative potential of every employee through teamwork and collaboration. Our technologies touch millions of lives every day, and this inspires us to do our best work – every day. By using your talent, ambition and creativity, you can build a career that allows you to make a real difference in people’s lives. You’re just one click away from the most impactful work you’ll ever do. Apply now and join our mission to help save lives. Someone, somewhere, will be glad you did.



We're driving toward the ultimate victory: a world without the fear of cancer.

Yor Primary Responsibilties as Verification Engineer:

  • Develops, evaluates, revises, and applies technical quality assurance protocols/methods to inspect and test in-process raw materials, production equipment, and finished products.
  • Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations.
  • Performs analysis and identifies trends in the inspection of finished products, in-process materials and bulk raw materials, and recommends corrective actions when necessary.
  • Ensures that established manufacturing inspection, sampling and statistical process control procedures are followed.
  • May assure compliance to in-house and/or external specifications and standards, such as GMPs and ISO regulations.
  • Evaluates and analyzes the efforts in organizing, documenting, and interpreting inspection support documents and records.

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We're unleashing the power of technology and human ingenuity to achieve new victories in the fight against cancer. Join us and have a global impact.

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23.10.2019
Position with re­spon­si­bil­i­ties, 100%

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Varian Medical Systems International AG

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