Senior Quality Engineer – Redmond, Oregon 

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Located in Bend, OR, OR

Salary: Competitive Comp & Benefits!

Senior Quality Engineer – Redmond, Oregon 

We are partnering with a top-notch Central Oregon employer to fill a Senior Quality Engineer position.  This is a contract role for 6+ months with the ability to go long-term. 

Who We Are
We are a growing, innovation-driven organization focused on delivering high-quality, compliant products in a highly regulated environment. Our team is committed to continuous improvement, strong collaboration, and building systems that support long-term success. If you enjoy improving processes, driving quality, and making a real impact, this is an opportunity worth exploring.

What You Get to Do!

• Lead quality initiatives across production and product development
• Develop and implement process control, validation, and inspection methods
• Design and execute experiments to identify process variation and improve outcomes
• Analyze data using statistical process control (SPC) to drive decisions
• Investigate non-conformances and lead corrective/preventive actions (CAPA)
• Partner with suppliers to resolve quality issues and improve performance
• Support design control, risk management, and regulatory compliance efforts
• Build and maintain key documentation (DHF, DMRs, technical files, etc.)
• Collaborate with internal teams and external labs on product testing
• Act as a quality leader and resource across cross-functional teams
• Take ownership of quality systems and influence real change
• Work cross-functionally with engineering, operations, and suppliers
• Be part of a team that values accountability and continuous improvement
• Contribute to product development and regulatory strategy
• Step into a leadership role, even without direct reports
• Help build and refine processes in a growing environment 

What You Will Bring…

• Bachelor’s degree in Engineering, Science, Math, or related field
• 4+ years of experience in Quality or Engineering
• Strong experience with quality systems and regulatory standards (ISO, FDA, etc.)
• Hands-on experience with CAPA, SPC, process validation, and root cause analysis
• Ability to work independently and drive projects forward
• Strong analytical and problem-solving skills
• Experience working cross-functionally and influencing teams
• Advanced Excel skills (data analysis, reporting, dashboards)
• Preferred experience in medical devices, pharma, or regulated industries

To Apply:

For consideration, please submit your resume to: natasha.cagle@expresspros.com

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