Mgr, Product Verification
Varian Medical Systems
Daettwil AG, Switzerland
vor 1 Tg.

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

As a member of our international product quality department comprising engineers and clinical staff, you will be working on the improvement of our products.

You will be involved in the verification and validation processes of our demanding and exciting global projects.

For that, you will be using the treatment devices at our in house test facilities and various radio oncological software packages.

You will also cooperate closely with teams at other development centers in Europe, and North America.

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

Imagine a world without fear of cancer. At Varian, that’s what we do, every day. We’re a company that is unleashing the power of technology and human ingenuity to achieve new victories in the fight against cancer When you join Varian, you’re joining a global company with over $3 billion in annual revenue, and some 9,200 team members across 70 countries around the world.

You’ll enjoy a culture that seeks to foster your creative potential and inspire you to do your best work. Bring your talent to a place that is making a difference in people’s lives.

The Product Verification Manager will lead a team based out of our office in Daettwil AG, Switzerland. As a leader of our international product verification team, you will be driving the improvement of our products.

You will be involved in the verification processes of our innovative and exciting global projects.

For that, you will be using the treatment devices at our in-house test facilities and various radio oncological software packages.

You will also cooperate closely with teams at other development centers in Europe, and North America.

The main purpose of the job holder will be to direct the activities of a product quality assurance function. You will develop quality standards for company products and oversee the development and execution of test plans and analysis of test results.

You will strive to automate test case execution where possible.

Specific Responsibilities

  • Lead and manage the product quality team who are responsible for the verification of our medical device applications
  • Follow the advances in testing, propose and drive improvements to processes
  • Develop test strategies and create test plans in close collaboration with your team, engineering, project management and others.
  • Report testing progress and take responsibility for the deliverable's as specified in the project plans
  • Design and execute test cases based on requirements, use cases, customer feedback
  • Ensure processes are followed and quality standards are met
  • Collaborate with Palo Alto and Baden teams
  • Desired Qualification

  • Management qualification and experience in medical device industry
  • Bachelor or master’s degree in computer science, medical engineering or equivalent skills
  • Five or more years of professional experience in software testing
  • 3 years management experience or supervisory equivalent.
  • Tester certification (ISTQB / SAQ Certified Tester) is a plus
  • Experience in regulated environment is an advantage
  • Strong analytical skills, creative, innovative and open minded
  • Fluency in German and English, both written and spoken
  • International Travel : approx. 5-10%
  • Flexibility in working hours
  • 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.

    LI-OS1

    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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