Senior Manufacturing Engineer

Posted 3 Days Ago
Be an Early Applicant
Salt Lake City, UT, USA
In-Office
100K-125K Annually
Senior level
Aerospace
The Role
Provides technical leadership for FDA-regulated medical device manufacturing. Leads process development, IQ/OQ/PQ validation, optimization, design transfer, new product introduction, fixture and tooling design, CAPA and NCR investigations, continuous improvement, audits, and capital equipment projects. Ensures compliance with FDA and ISO requirements while mentoring engineering and manufacturing personnel and improving production quality, efficiency, and repeatability.
Summary Generated by Built In

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.


Job Title:

Senior Manufacturing Engineer

Reporting To:

Manager, Operations Engineering

Work Schedule:

Onsite – Salt Lake City, UT

The Senior Manufacturing Engineer provides technical leadership for manufacturing operations supporting FDA-regulated medical devices. Supporting production, quality, and new product introduction activities, this role is responsible for developing, validating, and optimizing manufacturing processes to ensure product quality, regulatory compliance, and operational efficiency.


Key priorities include leading manufacturing process validations, supporting quality system investigations, driving continuous improvement initiatives, managing capital equipment projects, and providing technical leadership across manufacturing operations. This position plays a critical role in ensuring compliance with FDA and ISO requirements while supporting the successful introduction and manufacture of medical device products.


To be considered for the Senior Manufacturing Engineer role, here’s what you’ll typically need to bring with you:


  • 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.

As a Senior Manufacturing Engineer, you will:


  • 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.

How we care for you:


  • 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.

#LI-TB2

Salary Range Transparency:

Salt Lake City, UT $100,000.00–$125,000.00 Annually

Salary Range Disclaimer

The base salary range represents the low and high end of the Moog salary range for this position in the given work location. Actual salaries will vary depending on factors including but not limited to location, experience, and performance. The range(s) listed is just one component of Moog's total compensation package for employees. Other rewards may include annual bonuses, employee stock purchase plan, an open paid time off policy, and many region-specific benefits. 


This position requires access to U.S. export-controlled information.


Moog offers an inclusive workplace, and, as such, affirms the right of every person to participate in all aspects of employment based on merit without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. If you are interested in applying for employment and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department via phone at 844-367-5787.


No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our Talent Acquisition Team and have signed terms in place prior to any submittal. Absent compliance with these pre-conditions resumes submitted directly to any Moog Inc. employee or affiliate will not qualify for fee payment, and therefore become the property of Moog Inc.

Skills Required

  • Bachelor's degree in an engineering discipline
  • 7+ years of manufacturing engineering experience
  • 5+ years of experience in FDA-regulated medical device manufacturing
  • Experience leading IQ/OQ/PQ process validations
  • Knowledge of FDA QSR/QMSR requirements
  • Knowledge of ISO 13485 requirements
  • Knowledge of ISO 14971 requirements
  • Experience supporting CAPA, NCR, complaint investigations, and root cause analysis
  • Proficiency with SPC, process capability analysis, Gage R&R, DOE, and Minitab
  • Experience designing fixtures and optimizing manufacturing processes
  • Proficiency with SolidWorks or equivalent 3D CAD software
  • Experience with Design for Manufacturability, Design Transfer, and new product introduction
  • Strong project management and leadership skills
  • Six Sigma Green Belt or Black Belt certification
  • Experience with electromechanical medical devices or cleanroom manufacturing
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The Company
HQ: East Aurora, NY
7,850 Employees
Year Founded: 1951

What We Do

We work on some of the world’s most exciting technical projects, creating products that challenge the limits of what’s possible, from cutting-edge medical technology to space vehicles. Our formula includes one simple, surprising low-tech element that makes us stand out from everyone else: Trust. We trust each other to work hard and do the right thing. We give people credit for their ideas. We take pride in sticking with a problem until it’s solved. We value you for who you are as much as what you can do. We enjoy what we do. And you can do it, too.

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