Senior Quality Engineer

A Day in the Life

The Operations Quality team partners with manufacturing, engineering, and technical functions to ensure compliance, process capability, product quality, and continuous improvement across manufacturing operations. This position is based in West Valley, Utah and requires an onsite work schedule five (5) days per week at the manufacturing facility.

As a Senior Quality Engineer, you will provide quality engineering support for manufacturing operations with a primary focus on process validation and quality system execution. This role partners closely with engineering and manufacturing teams to ensure compliant, effective, and sustainable manufacturing processes while driving product quality, process reliability, and regulatory compliance within a highly regulated medical device environment.

Primary Responsibilities

• Lead process validation activities across the full validation lifecycle, including planning, protocol development, execution, analysis, reporting, and ongoing process monitoring.
• Partner with manufacturing and engineering teams to develop, implement, and maintain quality standards, controls, and manufacturing process requirements.
• Drive root cause investigations, corrective and preventive actions (CAPA), and nonconforming material (NCMR) activities to resolve quality issues and prevent recurrence.
• Analyze quality and process performance data using statistical methods to support risk-based decision making and continuous improvement initiatives.
• Develop and implement inspection, testing, and evaluation methods to verify product quality and manufacturing process capability.
• Support qualification and validation of manufacturing equipment, processes, and test methods.
• Ensure quality documentation, validation records, and manufacturing practices comply with applicable regulatory and quality system requirements.
• Mentor quality and engineering colleagues and provide technical leadership on complex quality and validation projects.

Required Qualifications

• Bachelor's degree in Engineering, Science, or technical field with 4+ years of engineering and/or quality experience OR Master's degree in Engineering, Science, or technical field with 2+ years of engineering and/or quality experience OR PhD.

Preferred Qualifications

• Bachelor's degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, or related engineering discipline; advanced degree preferred.
• Experience leading process validation activities for complex manufacturing processes in regulated environments.
• Experience with FDA-regulated medical device or pharmaceutical manufacturing.
• Experience using statistical analysis tools such as Minitab to support process improvement and quality decision making.
• Knowledge of Code of Federal Regulations (CFR) requirements, engineering drawings, machining, chemical processing, packaging, and sterilization processes.
• ASQ Certified Quality Engineer (CQE), Lean Six Sigma certification, or similar quality certification.
• 2+ years of experience executing process validation activities across the full validation lifecycle.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.