Sr Supplier Quality Engineer
$139.18k - $191.38kSiemens Healthineers
Sr Supplier Quality Engineer
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).
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 in healthcare and medical technology sector and strong understanding of ISO13485 and ISO9001
- Experience driving improvements in a PPAP/APQP environment where suppliers share in the quality data and monitoring techniques
- 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 with lean manufacturing, statistical process control, Six Sigma, and design for manufacturability practices.
- Strong track record of problem solving and driving process improvements
- Passion for Travel and Onsite Supplier Engagement. Willingness to travel This role will require travel to supplier locations both domestically and internationally, minimum of 30-40%, potentially on short notice.
- Proven strong communicator with internal and external partners
- Familiarity with eQMS including: quality management systems, quality management software and ERP systems (SAP preferred)
What Will Set You Apart:
- One or more of the following certifications: Certified Quality Engineer, Six Sigma Black Belt, ISO Certified Lead Auditor
To find out more about Siemens Healthineers businesses, please visit our company page here.
The base pay range for this position is:
$139,180 - $191,378
Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.
Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.
EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.
Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.
If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you're unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at View email address on click.appcast.io. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.
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Export Control: "A successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations."
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