Senior Manufacturing Engineer

About the role

Moog is a performance culture that empowers people to achieve great things. Our people enjoy solving interesting technical challenges in a culture where everyone trusts each other to do the right thing. For you, working with us can mean deeper job satisfaction, better rewards, and a great quality of life inside and outside of work.

Responsibilities

• Provide technical leadership and mentorship to engineers, technicians, and manufacturing personnel.
• Lead the development, qualification, validation, and optimization of manufacturing processes to support production, quality, and regulatory requirements, including IQ/OQ/PQ validation activities.
• Support CAPA, NCR, and complaint investigation activities by conducting root cause analysis and implementing corrective actions.
• Identify and implement process improvements that enhance manufacturing efficiency, quality, and operational performance.
• Lead design transfer and new product introduction activities, partnering with cross-functional teams to successfully transition products into manufacturing.
• Design and develop fixtures, tooling, and test equipment to improve manufacturing capability and process repeatability.
• Drive Lean Manufacturing and continuous improvement initiatives utilizing statistical methods and best practices.
• Support internal and external audits and ensure compliance with FDA and ISO quality system requirements.
• Manage capital equipment projects including specification development, procurement, implementation, and validation.

Requirements

• Bachelor’s degree in an Engineering discipline and 7+ years of manufacturing engineering experience.
• 5+ years of experience in FDA-regulated medical device manufacturing preferred.
• Experience leading IQ/OQ/PQ process validations.
• Strong knowledge of FDA QSR/QMSR, ISO 13485, and ISO 14971 requirements.
• Experience supporting CAPA, NCR, complaint investigations, and root cause analysis activities.
• Proficiency with statistical analysis tools and methodologies including SPC, process capability analysis (Cp/Cpk), Gage R&R, DOE, and Minitab.
• Experience designing fixtures and implementing manufacturing process optimization initiatives.
• Proficiency with SolidWorks or equivalent 3D CAD software.
• Experience with Design for Manufacturability (DFM), Design Transfer, and new product introduction activities.
• Strong project management and leadership skills with the ability to lead cross-functional engineering projects.
• Six Sigma Green Belt or Black Belt certification is preferred.
• Experience with electromechanical medical devices and/or cleanroom manufacturing is preferred.

Benefits

• Financial Rewards: Great compensation package, annual profit sharing, matching 401(k), Employee Stock Purchase Plan, Flexible Spending Accounts, and Health Savings Accounts.
• Work/Life Balance: Flexible paid time off, company holidays, parental leave program, and relocation assistance.
• Health & Welfare: Comprehensive medical, dental, vision, life, disability, Employee Assistance Program (EAP), and supplemental benefit coverage.
• Professional Skills Development: Tuition assistance, mentorship, coaching opportunities, leadership development programs, and ongoing career growth support.
• Collaborative and Welcoming Workplace: Inclusive culture rooted in our values, supported by Employee Resource Groups and team-building activities.
• Additional site-specific benefits may be available.

Pay

Salary Range: $100,000.00–$125,000.00 Annually (Salt Lake City, UT)

Schedule

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