Quality Systems Engineer

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Varian Medical Systems, a Siemens Healthineers company, is seeking a Quality
Engineer to join our team in Austin, Texas.

As the site's primary quality
engineering resource, you will have the opportunity to contribute to important
engineering decisions and directly support manufacturing operations, incoming
inspection, supplier quality, quality systems, and continuous improvement
activities within an ISO 13485:2016 -compliant manufacturing environment.
Working closely with Supply Chain, Engineering, Regulatory Affairs, IT, and other
cross-functional teams, the Quality Engineer will help develop, implement, and
sustain scalable quality practices that ensure product quality, process
effectiveness, regulatory compliance, and operational excellence.
The Quality Engineer will provide hands-on support for manufacturing quality,
nonconformance and CAPA processes, quality systems administration, and
operational improvement initiatives.

Leveraging quality engineering tools, data-
driven decision-making, and structured problem-solving methodologies, this role will identify risks, drive corrective and preventive actions, and establish
practical, sustainable quality controls that support the continued growth and
success of the Austin, TX operation.
What You will do:


* Serve as a key quality engineering resource across quality systems, and operational excellence initiatives.


* Define, implement, maintain, and continuously improve quality system processes, procedures, work instructions, and other related controlled documentation to support Austin operations and ISO 13485:2016 compliance.


* Support manufacturing operations by ensuring products, processes, and quality controls meet established specifications, regulatory requirements, and customer expectations.


* Investigate, document, and support the timely closure of nonconforming materials, components, processes, and finished goods while partnering with Operations, Engineering, Supply Chain, and other stakeholders to drive timely resolution.


* Lead and support root cause investigations, containment actions, corrective and preventive actions (CAPA), and recurrence prevention efforts using structured problem-solving methodologies.


* Analyze quality system data to identify trends, mitigate risks, and drive data-based improvements.


* Establish, monitor, and report key quality performance indicators, including yield, defect trends, supplier performance, inspection effectiveness, calibration compliance, and issue closure metrics.


* Support new product introductions, manufacturing readiness activities, p...