Senior Manager, Quality Engineering & Quality Assurance

Posted 12 Days Ago
Be an Early Applicant
Salt Lake City, UT, USA
In-Office
Senior level
Healthtech • Pharmaceutical
The Role
Manage metals quality engineering and assurance: oversee in-process and finished-goods inspection, audits, CAPA/NCR management, failure investigations, regulatory compliance (FDA QSR, ISO 13485), and continuous improvement using Lean/Six Sigma. Lead and develop supervisors and quality teams, coordinate cross-functional projects, support product release documentation and inspection readiness.
Summary Generated by Built In

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 Senior Manager, Quality Engineering & Quality Assurance position is a unique career opportunity that could be your next step towards an exciting future.

The Senior Manager, Quality Engineering & Quality Assurance will manage the Metal Manufacturing team to ensure smooth and continuous operations of site quality system, quality control and assurance inspection for in process and finished goods. Oversee process audits and final product release documentation. Advise and facilitate failure investigations, compliance methodologies for manufacturing of Metal Components. Manage team with activities that focus on implementing and optimizing quality engineering practices while ensuring a culture of quality and compliance with global regulatory requirements.

How You'll Make an Impact:

  • Quality representative for Metals associated with internal and external audits. Coordinate with Draper Quality Systems Management for audit preparation, execution and action plans. Ensure Metals Organization executes to Draper site quality objectives/plans
  • Manage supervisors and/or oversee the work of assigned quality assurance team within own function, one or more production line or projects. Develop a robust talent development plan in alignment with functional growth strategies of the department. Identify opportunities and lead the implementation of changes to drive improvements 
  • Manage quality assurance project activities (e.g., CAPA) with the accountability for successful completion of all deliverables to the business within established schedule, scope and quality objectives including training, approvals, and system effectiveness. Identify risk, develop mitigation strategies, alternative solutions, resolve issues, action item follow up, etc. in collaboration with cross functional groups 
  • Collaborate with cross-functional groups to manage inspection of in-process and finished goods, assemblies and components including proper implementation 
  • Negotiate solutions with cross-functional groups (e.g., Manufacturing Operations, Supply Chain, and Engineering) for continuous improvement 
  • Manage project activities with the accountability for successful completion of all deliverables to the business and develop project plans, schedule, scope and objectives while using engineering methods (e.g., SIX Sigma and LEAN methods), employing technical design skills to re-design/design on new products and/or processes. Identify risks, develop mitigation strategies, define alternative solutions, resolve issues, and follow-up on action items in collaboration with cross functional groups 
  • Manage and/or oversee the work of assigned team within own function and/or cross functional project teams and may have some budgetary responsibilities. Develop a robust talent development plan in alignment with functional growth strategies of the department 
  • Provide technical guidance to cross-functional and/or departmental groups to develop and provide design recommendations that integrate into component(s) or product(s) with moderate complexity. Collaborate with Campus Model shared services to support Draper Metals Organization. 
     

What You'll Need (Required):

  • Bachelor's degree in related field related experience in Materials, Chemical, Mechanical and/or Metals engineering.
  • Experience in Quality Engineering or Quality Management within the medical device industry with demonstrated Product Quality decision-making, or equivalent work experience based on Edwards’ criteria.
  • Demonstrated track record in management of technical and/or engineering disciplines in a dynamic Quality/Manufacturing Environment.
     

What Else We Look For (Preferred):

  • Technical quality leadership experience supporting metals manufacturing, metal components, or precision-manufactured components.
  • Experience supporting commercial production quality for processes such as machining, forming, chemical processing, laser cutting, tubing, nitinol, or other metal component manufacturing processes.
  • Demonstrated experience leading both Quality Engineering and Quality Assurance functions, including oversight of NCRs, CAPAs, TMVs, inspection readiness, product release, and quality metrics.
  • Experience managing Supervisors and associated direct and indirect manufacturing inspection and/or testing resources.
  • Experience managing or partnering closely with inspection, quality control, and manufacturing operations teams to ensure in-process and finished goods meet quality, compliance, and release requirements.
  • Medical Device external audit leadership experience
  • Proven ability to serve as a quality representative during internal, notified body, FDA, customer, or external regulatory audits, including audit preparation, execution, response, and action plan management.
  • Strong working knowledge of applicable medical device quality system and regulatory requirements, including FDA Quality System Regulation, ISO 13485, GMP, and global quality standards.
  • Experience using quality engineering tools and statistical methods such as process capability, statistical process control, FMEA, DOE, test method validation, root cause analysis, Lean, and Six Sigma.
  • Demonstrated ability to lead technical quality investigations, drive risk-based decision-making, and implement sustainable corrective and preventive actions in a high-volume or complex manufacturing environment.
  • Experience developing and using quality metrics, management review inputs, and operational dashboards to monitor trends, communicate risks, and drive continuous improvement.
  • Certified Quality Engineer, Six Sigma Black Belt, Lean certification, or equivalent quality/manufacturing certification.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Skills Required

  • Bachelor's degree in Materials, Chemical, Mechanical, Metals engineering or related field (or equivalent related experience).
  • Experience in Quality Engineering or Quality Management within the medical device industry with demonstrated product quality decision-making.
  • Demonstrated track record managing technical and/or engineering disciplines in a dynamic Quality/Manufacturing environment.
  • Technical quality leadership supporting metals manufacturing or precision-metal components (machining, forming, chemical processing, laser cutting, tubing, nitinol).
  • Experience leading Quality Engineering and Quality Assurance functions, including oversight of NCRs, CAPAs, TMV, inspection readiness, product release, and quality metrics.
  • Experience managing supervisors and direct/indirect manufacturing inspection and testing resources.
  • Experience partnering with inspection, quality control, and manufacturing operations to ensure in-process and finished goods meet quality and release requirements.
  • Medical device external audit leadership experience and ability to serve as quality representative for internal, notified body, FDA, customer, or external regulatory audits.
  • Strong working knowledge of FDA Quality System Regulation, ISO 13485, GMP, and global quality standards.
  • Experience using quality engineering tools and statistical methods: process capability, SPC, FMEA, DOE, test method validation, root cause analysis, Lean, Six Sigma.
  • Demonstrated ability to lead technical investigations, drive risk-based decision-making, and implement sustainable corrective and preventive actions.
  • Experience developing and using quality metrics, management review inputs, and operational dashboards to monitor trends and drive improvement.
  • Relevant certifications (e.g., Certified Quality Engineer, Six Sigma Black Belt, Lean certification) or equivalent manufacturing/quality certification.

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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