Sr Manager, Process Engineering

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Varian Medical Systems, a Siemens Healthineers company is hiring for a Sr Manager, Process Engineering.

In this role you will lead global manufacturing process governance to ensure the organization delivers compliant, high-quality products through standardized and controlled processes.

You will own global manufacturing quality system documentation and the engineering change process, driving consistency, audit readiness, and execution discipline across all sites.



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*This role is designed to be onsite at one of our manufacturing locations: Palo Alto, California; Kemnath, Germany; Haan, Germany; Baden, Switzerland; Beijing, China

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*What You will do:


* Own global manufacturing quality system documentation and represent Varian in internal and external audits (e.g., ISO 13485, MDSAP) as process owner for areas including Production Process Controls (PPC), Resource Management (RMT), and related procedures, ensuring consistent application across all sites


* Establish and govern document lifecycle management, including creation, revision, approval, and periodic review


* Drive global standardization of processes, resolving site-level variation and ensuring alignment to defined requirements


* Own the end-to-end engineering change management execution, ensuring changes are controlled, timely, auditable, and effective in resolving underlying issues


* Lead a multi-functional team including process engineering, change management, program management, and drafting (via a functional manager), ensuring alignment between process definition, documentation, and execution


* Establish and monitor KPIs for change management performance, including cycle time and implementation effectiveness


* Prepare and coach manufacturing engineering teams for audits, including readiness reviews and gap closure


* Drive alignment across Manufacturing, Engineering, Quality, and Supply Chain to implement systemic improvements across sites, even where direct ownership is distributed


* Drive continuous improvement of global processes, incorporating lessons learned from audits, deviations, and performance gaps


* Identify and resolve systemic issues in process execution, documentation quality, and change management effectiveness through projects and the CAPA process


* Translate manufacturing and quality performance data into prioritized, actionable improvements, ensuring alignment between process control updates, change execution, and reduction of systemic non-conformances

What You will have:


* Deep understanding of manufacturing quality systems, including PPC,...