Sr Supplier Quality Engineer (onsite)

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 a Sr Supplier Quality Engineer onsite at our HQ In Palo Alto, California. In this role you will ensure and improve the supplier quality in the assigned area of dedicated business (Medical Device products and services). **This role is designed to be completed onsite in Palo Alto, California** What You will do: Own Site-Level Supplier Performance Manage assigned suppliers to ensure alignment with quality and operational requirements across QII, Manufacturing, Installation, and Field Service. Ensure Quality and Operational Continuity Identify and mitigate supplier quality risks, manage Qnotes and MRB processes, and minimize scrap, disruption, and field impact. Lead Supplier Management and Improvement Efforts Drive daily supplier communication, performance monitoring (e.g., dashboards, KPIs), compliance to standards, and targeted improvement initiatives. Partner Cross-Functionally to Drive Results Collaborate with Production, Manufacturing Engineering, Procurement (strategic and operational), Service, SQMs, and SMEs to resolve issues, support operations, and improve efficiency. Participate in AVM and related forums to ensure timely resolution of non-conformances. Support New Product Introduction (NPI) and Specification Alignment Engage in NPI processes to ensure manufacturability, clear specifications, and supplier alignment using QATS tools. Partner with Engineering and suppliers to define critical attributes, acceptance criteria, and inspection strategies (FAI, PSI). Drive Supplier Quality Improvement and Issue Resolution Act as the SME for assigned suppliers, leading root cause analysis, SCAR processes, and corrective actions. Track and close supplier issues, manage Supplier Change Notifications (SCN), and reduce defects impacting manufacturing, installation, and service. Implement Quality at the Source (QATS) Guide suppliers in adopting QATS tools (e.g., PFMEA, SPC, MSA, Cpk, Control Plans) to improve process control, increase part acceptance, and shift from inspection to data-driven validation. Monitor Field Performance and Escalate Risks Partner with Service teams to analyze field data, drive supplier root cause and corrective actions, and communicate emerging risks, status, and mitigation plans clearly to stakeholders. Reduce Cost of Poor Quality Analyze and reduce non-conformance and warranty costs by identifying trends, addressing root causes, and implementing sustainable improvements. Conduct Supplier Audits and Ensure Compliance Perform for-cause audits, identify root causes, drive corrective actions, and ensure ongoing compliance with quality and regulatory requirements. What You will Have: Bachelor of Engineering in Electrical, Mechanical, Industrial, or Biomedical, fields OR equivalent experience. 8+ years of technical leadership experience in Supply Chain engineering, design engineering and/or Supplier Quality Engineering. Experience supporting medical device products in an FDA-regulated and ISO 13485 quality environment. Hands-on experience with PPAP/APQP principles and supplier process controls such as FMEA/PFMEA, Control Plans, SPC, MSA, Cpk/Ppk, process capability, and process validation. Ability to lead projects consisting of cross-functional teams, and manage complex problem solving projects with excellent communication and interpersonal skills. Proficient in understanding supplier manufacturing process, engineering requirements, and design solutions in a regulated industry. Understanding of supplier controls necessary to ensure design specs are met and adhered to Experience w…

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