Manual qa tester h1.location_city

Together, we can beat cancer.

At Varian, a Siemens Healthineers Company, we bring together the world's best talent to realize our vision of a world without fear of cancer. Together, we work passionately to develop and deliver easy-to-use, efficient oncology solutions.

We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.

If you want to be part of this important mission, we want to hear from you.

Varian is looking for a QA Engineer to join our team in San Jose, California. In this position you would be expected to perform assignments independently by applying Good Manufacturing Practices in all areas of responsibility to ensure our customers receive the highest possible quality products. This position is responsible for Incoming Inspection activities, interactions with internal customers to ensure parts are inspected in a timely manner in a FDA 21 QSR 820 and ISO 13485 regulated environment. You would be expected to perform all assigned duties and conduct business in a professional manner.

What You will do:

• Design, implement and maintain quality assurance protocols and methods for processing materials into partially finished or finished products.
• Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution.
• Design methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products.
• Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.
• May assure compliance to in-house and/or external specifications and standards (i.e. GLP, GMP, ISO, Six Sigma).

What You will have:

• Typical Education and Experience: Bachelors degree (or equivalent experience) and 5 years of related experience or Masters Degree with 3 years of related experience.
• Experience with Optical Gaging Products (e.g. Calypso, Keyenc, Zone3)
• Experience with CMM or other vision systems
• Experience with GD&T
• Minimum Required Skills and Knowledge: Proficient in utilizing business tools such as: E-mail, Microsoft Word, Excel, and PowerPoint. Experience with HCM (e.g., Workday) or equivalent ERP product and productivity software desired.

#LS-OS1

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