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Manager Manufacturing Excellence information

What is a Manager Manufacturing Excellence?

A Manager Manufacturing Excellence is a professional responsible for leading and implementing continuous improvement initiatives in a manufacturing environment. Their main goal is to optimize production processes, enhance operational efficiency, and promote best practices to achieve higher quality and productivity. They often use methodologies such as Lean, Six Sigma, and Kaizen to identify areas for improvement, train teams, and drive a culture of excellence throughout the organization. This role also involves collaborating with different departments to ensure alignment with company goals and regulatory standards.

What does a Manager Manufacturing Excellence do?

A Manager Manufacturing Excellence leads continuous improvement by facilitating Lean, Six Sigma, or similar methodologies within production teams. This involves conducting process audits, gathering and analyzing performance data, and collaborating closely with operators, engineers, and supervisors to identify inefficiencies or bottlenecks. The manager often organizes training sessions and workshops to build a culture of problem-solving and accountability. Regularly, they champion cross-functional projects and ensure that best practices are shared and sustained across departments.

What are the key skills and qualifications needed to thrive as a Manager Manufacturing Excellence?

To thrive as a Manager Manufacturing Excellence, you need expertise in lean manufacturing, process optimization, and a solid background in industrial engineering or a related field. Familiarity with Six Sigma methodology, ERP systems, and quality management certifications like Lean Six Sigma Black Belt are typically required. Strong leadership, analytical thinking, and effective communication set outstanding candidates apart in driving continuous improvement. These skills are crucial for enhancing operational efficiency, reducing costs, and fostering a culture of excellence within manufacturing organizations.

What is the difference between Manager Manufacturing Excellence vs Manufacturing Engineer?

AspectManager Manufacturing ExcellenceManufacturing Engineer
CredentialsBachelor's degree in engineering or related field; certifications in Lean, Six Sigma often preferredBachelor's degree in engineering, manufacturing, or industrial engineering
Work EnvironmentLeadership role overseeing process improvements, cross-functional teams, strategic initiativesTechnical role focused on designing, developing, and implementing manufacturing processes
Industry UsageCommonly used in manufacturing companies focusing on process optimization and operational excellenceUsed across manufacturing sectors for process development and technical support

The Manager Manufacturing Excellence focuses on leading process improvement initiatives and strategic operational excellence, while the Manufacturing Engineer concentrates on technical process design and implementation. Both roles require engineering credentials and are integral to manufacturing success, but they differ in scope and responsibilities.

What are the most commonly searched types of Manufacturing Excellence jobs in Utah?

The most popular types of Manufacturing Excellence jobs in Utah are:

What job categories do people searching Manager Manufacturing Excellence jobs in Utah look for?

The top searched job categories for Manager Manufacturing Excellence jobs in Utah are:

What cities in Utah are hiring for Manager Manufacturing Excellence jobs?

Cities in Utah with the most Manager Manufacturing Excellence job openings:

Manager, Manufacturing Quality

Salt Lake City, UT • On-site


Edwards Lifesciences
Medical Equipment and Supplies Manufacturing • 10K+ employees

8.2

Company rating: 8.2 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

84th of 545 rated manufacturers

People enjoy working here

Good employer

Paid breaks


$120 - $160/hr

Other

Posted 13 days ago


Job description

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Manager, Manufacturing Quality position is a unique career opportunity that could be your next step towards an exciting future.

The Manager, Manufacturing Quality is responsible for leading Quality Assurance and supporting commercial Metals Manufacturing operations. This role provides leadership and oversight for inspection, testing, nonconformance management, product disposition, quality data review, and compliance activities to ensure product quality, operational excellence, and regulatory compliance. The position partners closely with Manufacturing, Engineering, Supply Chain, and Quality stakeholders to drive timely resolution of quality issues and continuous improvement across commercial production operations.

How You Will Make An Impact
  • Lead Quality Assurance activities and support commercial Metals Manufacturing operations, ensuring compliance with quality system requirements and regulatory standards.
  • Direct and develop a team of quality supervisors, inspectors, and quality professionals to support manufacturing operations, product inspection, testing, and release activities.
  • Provide leadership and oversight for nonconformance investigations (NCRs), ensuring timely evaluation, containment, disposition, root cause investigation, and closure.
  • Establish and maintain quality inspection and testing strategies for in-process and finished products to ensure compliance with product specifications and quality requirements.
  • Partner with Manufacturing, Engineering, Supply Chain, and Quality Engineering teams to resolve quality issues, support production objectives, and drive continuous improvement initiatives.
  • Oversee product quality disposition activities, including product holds, release decisions, and escalation of quality risks when appropriate.
  • Monitor and analyze quality performance metrics and operational trends, providing data-driven recommendations to improve product quality, compliance, and manufacturing performance.
  • Ensure inspection processes, testing activities, and quality documentation comply with internal procedures and applicable regulatory requirements.
  • Support internal and external audits, regulatory inspections, and management reviews through preparation, execution, and follow-up activities.
  • Develop team capabilities through coaching, performance management, succession planning, and technical skill development.
  • Identify and implement process improvements to enhance efficiency, effectiveness, and compliance within the Quality Assurance organization.
What You’ll Need (Required)
  • Bachelor's degree in engineering or scientific disciplines
  • Experience within Quality Assurance, Quality Engineering, Manufacturing Quality, or Operations Quality in Medical Device manufacturing; or equivalent experience based on Edwards' criteria.
  • Experience directly leading people, including supervisors, inspectors, technicians, and/or professionals.
What Else We Look For (Preferred)
  • Engineering or Science degree
  • Medical device manufacturing experience.
  • Experience leading Quality Assurance teams supporting commercial manufacturing operations.
  • Experience with nonconformance management (NCRs), product disposition, initiating and removing product holds, quality investigations, and root cause analysis.
  • Experience overseeing incoming, in-process, and finished goods inspection and testing activities.
  • Strong knowledge of FDA Quality System Regulation, ISO 13485, and Good Manufacturing Practices (GMP) as they relate to product realization and manufacturing.
  • Experience supporting audit readiness, regulatory inspections, and quality management reviews.
  • Working knowledge of statistical quality methods, quality metrics, and trend analysis.
  • Experience driving continuous improvement initiatives utilizing Lean, Six Sigma, or similar methodologies.
  • Experience using quality management systems and enterprise systems such as ETQ, JDE, PLM, SAP, or similar platforms.
  • ASQ CQE or other ASQ quality certifications.
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Edwards Lifesciences logo

About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958


What Edwards Lifesciences employees say

Pay

Benefits

Hours and flexibility

Workplace

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