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Siemens Healthineers
Validation Specialist (Radiation Therapy) ** Onsite - Palo Alto**
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What they do
A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
$101,424 / year median in California
+8% projected growth
Job Description
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Varian Medical Systems, a Siemens Healthineers company is hiring an on-site resource in Palo Alto, California. Our overall goal is to release quality products for clinical users to ensure an effective and safe treatment of patients as well as to ensure the needs of the operator and patient are implemented as expected. We are looking for people with current clinical backgrounds and excellent analytical abilities that can help us drive the quality of our development work. Do you have clinical experience in Radiation Oncology? We'd like to talk with you! The Validation Specialist is intended to represent the voice our of clinical users and patients from the radiation therapist/medical dosimetrist perspective by identifying clinical workflow bottlenecks, missed opportunities, annoyance in workflows, and critical features which may lead to mistreatments or hazards. Join the Product Validation team and use your analytical and logic skills to ensure that the medical devices being developed are of high quality, intuitive, and meet design and intended use requirements.
- This role is on-site in Palo Alto, California. Although there is some remote/hybrid allowance - the successful applicant needs to be located in the Palo Alto region or be willing to relocate if offered the position
- What You will do
- Ensure that validation is complete, and that Varian's products are safe, effective, and meet the user's intended use, with good objective test evidence prior to release.
- Evaluate and discuss clinical practices, treatment techniques and clinical process optimizations with Product Management, User Experience and Design Engineering teams to define new product requirements.
- Provide continuous feedback and implement improvements to the design, development, and modification of radiation and oncology products and systems.
- Support development and maintenance of Varian products, including Oncology Information Systems, Treatment Planning Management Systems, and Treatment Delivery and Imaging Systems.
- Define strategy for assuring thorough design validation of new products to demonstrate that they meet design and intended use requirements.
- Develop, modify, and execute design validation plans to meet product and system requirements.
- Participate in requirements analysis, use case development, and risk hazard analysis.
- Analyze and write test designs and procedures, establish traceability to requirements and risk mitigations.
- In addition to exploratory testing, consult with Product Verification Engineers, Product Marketing, User Exper.