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Quality System Manager
3 months ago
:Demonstrated expertise with FDA regulation, ISO 13485, ISO 14971, IEC 62304, MDSAP, IEC 60601, and applicable other medical device regulations.Working knowledge of software development lifecycle and SaMD regulations. Familiarity with radiotherapy equipment is preferred.Experience in managing/coordinating quality assurance activities in a cross-functional team environmentAbility to work and influence geographically diverse and international workgroups including excellent communication and intrapersonal skills.Travel may be required – domestically and internationally.Varian is required to comply with all local and applicable regulations that may be associated with vaccine requirements for certain roles.Fighting cancer calls for big ideas.We envision a world without fear of cancer. Achieving this vision takes dedication and commitment from all of us, every single day. That's why we celebrate and value the distinctly beautiful and intersectional identities of each of our employees. We are a mirror of our patient-base, which allows us to innovate. Big ideas come from everywhere, and the best ideas are fostered by our unique individual experiences. At Varian, we encourage you to bring your whole self to work and believe your bold and authentic perspective will help to power more victories over cancer.#TogetherWeFight