Manager, Quality Control Testing – Interventional Oncology

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Varian Medical Systems, a Siemens Healthineers company is hiring a Quality Control (QC) Testing Manager.

In this role you will be responsible for leading on-site QC testing operations supporting the Interventional Oncology (IO) business in Austin, Texas.

This role ensures that incoming materials, in-process samples, and finished medical devices meet defined specifications prior to release.

The QC Testing Manager drives compliance with Quality System Regulations, supports sterilization and biocompatibility activities, applies Statistical Process Control (SPC), and partners cross-functionally to ensure product quality, patient safety, and business continuity.



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*This position is leveled as aManagerrole designed to be onsite in Austin, TX.

The Scope includes:peopleleadership responsibility and execution-focused accountability

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What You will do:


* Lead daily QC testing operations supporting medical device manufacturing.


* Manage and develop QC testing staff, including training, qualification, and performance management.


* Ensure compliance with Quality System Regulations (QSR), internal procedures, and Good Documentation Practices.


* Review and disposition QC test results, deviations, OOS/OOT events, and investigations.


* Apply Statistical Process Control (SPC) methods tomonitorprocess performance, detect trends, and drive improvements.


* Support sterilization-related quality activities including review of records and acceptance criteria (Steam, EO, Gamma).


* Support biocompatibility-related testing activities, risk assessments, and documentation.


* Partner with Manufacturing, Engineering, Quality Assurance, Regulatory Affairs, and Supplier Quality.


* Act as QC SME during internal, customer, and regulatory audits.


* Drive continuous improvement initiatives to reduce variation, rework, and retesting.

What You will have:



* Bachelor's degree ina scientificor engineering discipline or equivalent experience.


* 8+ years of experience in Quality Control, laboratory operations, or medical device manufacturing.


* 3+ yearsof peopleleadership experience.


* Experience with medical device manufacturing and product release testing.


* Working knowledge of Quality System Regulations (QSR) and ISO 13485.


* Experience applying Statistical Process Control (SPC) techniques in a manufacturing environment.


* Strong problem-solving, communication, and cross-functional collaboration skills.

What will set You apart:



* Experience with sterilization methodologies: Steam, Ethylene Oxide (EO), and Gamma.
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