Quality Process Engineer - Medical Device Excellence
Varian Medical Systems
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Job summary
Varian is seeking a Quality Process Engineer to support process improvements across product development for cancer care solutions. You will work with cross-functional teams including Product, Project Management, Marketing, QA, Regulatory Affairs, R&D, Manufacturing, and Supply Chain to standardize workflows and ensure compliance in a global environment.
You will analyze needs, develop procedures and trainings, and implement standardized processes using content management systems to enable safe
Qualifications
- Bachelor’s degree in Engineering or a technical field.
- 3–4 years in the medical devices field.
- Proficient with Microsoft Office (Word, Excel, PowerPoint, Visio).
- Familiar with ISO 13485 and CFR 820.30 Design Controls.
- Experience authoring technical procedures and documentation.
Responsibilities
- Drive process changes and manage content for product development.
- Collaborate with cross-functional teams including QA, Regulatory, R&D, and Manufacturing.
- Analyze stakeholder needs and root causes to improve product lifecycle processes.
- Create and implement procedures, trainings, and frameworks to standardize workflows.
Skills
Education
Tools
Job description
Varian is seeking a Quality Process Engineer to support process improvements across product development for cancer care solutions. You will work with cross-functional teams including Product, Project Management, Marketing, QA, Regulatory Affairs, R&D, Manufacturing, and Supply Chain to standardize workflows and ensure compliance in a global environment.
You will analyze needs, develop procedures and trainings, and implement standardized processes using content management systems to enable safe
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