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Principal Quality Engineer, Advanced Catheters & Extrusions

Edwards Lifesciences

Irvine, CAFull-time$121–171K/yrSeen 6 days agoSeen in employer's feed 6 days ago

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At a glance

Compensation
$121–171K/yr
Location
Irvine, CA
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Principal Quality Engineer serves as a technical subject matter expert for Advanced Catheters and Extrusions programs, supporting development through commercialization. The role partners with engineering, manufacturing, operations, and quality teams across sites to guide product and process validation, statistical analysis, technical investigations, and manufacturing readiness. It also provides technical mentorship and supports robust products and manufacturing processes.

Skills & qualifications

RequiredNice to have

Skills

Test Method ValidationProcess ValidationEquipment ValidationIQ/OQ/PQRegulated Industry ExperienceMedical Device ExperienceClass II/III ProductsExtrusion ManufacturingPolymer ManufacturingMaterial Property TestingCatheter TechnologiesBalloon TechnologiesTechnology TransferProduct Development ProcessDesign ControlsRisk ManagementMaterial CharacterizationDesign CharacterizationSpecificationsTolerancingCross-Functional LeadershipProject ManagementStatistical MethodsCapability StudiesQuality EngineeringSix Sigma Black BeltLean Black Belt

Qualifications

Bachelor's in Engineering or Scientific Field + 6 Years or Master's in Engineering or Scientific Field + 5 Years6+ Years Quality or Related Engineering Experience or 5+ Years With Master'sCertified Quality EngineerSix Sigma Black Belt CertificationLean Black Belt Certification

Full job description

USA - California – Irvine

Full time

Req-51788

Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

The Principal Quality Engineer will serve as a Quality Engineering technical subject matter expert supporting Advanced Catheters and Extrusions Process Engineering programs from early-stage development through commercialization. In this highly cross-functional role, you will partner with R&D, Process Engineering, Manufacturing, Operations, and other Quality teams across multiple sites to provide technical leadership for new product development, new product introduction, pilot manufacturing, and technology transfer activities. You will apply Quality Engineering expertise to test method validation, process and equipment validation (IQ/OQ/PQ), material and design characterization, tolerancing, capability studies, and statistical analysis to support robust product and manufacturing processes.

You will make an impact by:

  • Serve as a Quality Engineering technical subject matter expert for Advanced Catheters and Extrusions programs, providing technical guidance throughout new product development, new product introduction, pilot manufacturing, and commercialization.

  • Lead Quality Engineering activities supporting the development and validation of products, manufacturing processes, equipment, and test methods, including Test Method Validation (TMV) and IQ/OQ/PQ activities.

  • Apply a data-driven and statistical approach to Quality Engineering decisions, including capability studies, data analysis, experimental results, and assessment of process and product performance.

  • Provide Quality Engineering expertise for extrusion, polymer, catheter, and balloon-related technologies, including evaluation of material properties, design requirements, tolerances, specifications, and associated product and manufacturing risks.

  • Partner cross-functionally with R&D, Process Engineering, Manufacturing, Operations, Supplier Quality, and other Quality teams to develop robust products and manufacturing processes and support successful program execution.

  • Collaborate across sites and with technical centers of excellence to support manufacturing readiness, validation, technology transfer, and commercialization activities.

  • Develop, review, and approve technical documentation including validation protocols and reports, specifications, test methods, risk-management documentation, process controls, and change-control documentation.

  • Lead and provide technical guidance for complex product, process, and Quality investigations, including nonconformances, CAPA, supplier quality issues, and other Quality or compliance matters.

  • Provide technical mentorship and guidance to engineers and technicians, helping build Quality Engineering capability and consistency across programs.

  • Other incidental duties

What you’ll need (Required):

  • Bachelor's degree in engineering or scientific related fields with a minimum of 6 years of experience in Quality Engineering, Manufacturing Quality, Process Engineering, or a related engineering discipline; OR Master's degree in engineering or scientific related fields with a minimum of 5 years of experience in these areas.

  • Demonstrated experience with Test Method Validation (TMV) and process/equipment validation, including IQ/OQ/PQ.

  • Highly regulated industry experience.

What else we look for (Preferred):

  • Medical device industry experience supporting Class II and/or Class III products.

  • Experience with extrusion and/or polymer manufacturing processes, including material property testing and analysis.

  • Experience supporting catheters, balloon, extrusion, or other polymer-based medical-device technologies.

  • Experience with technology transfer and supporting products or manufacturing processes from development through pilot production, validation, manufacturing readiness, and commercialization.

  • Knowledge of or experience with Product Development Process (PDP), Design Controls, and risk management.

  • Experience with material- and design-related characterization, including an understanding of specifications and tolerancing.

  • Experience leading cross-functional technical teams or projects and partnering effectively across multiple sites.

  • Project management experience supporting complex product development or manufacturing programs.

  • Experience applying statistical methods to capability studies, validation activities, and technical decision-making.

  • Experience providing Quality Engineering support within a development, pilot manufacturing, laboratory, or Center of Excellence environment.

  • Certified Quality Engineer (CQE), Six Sigma Black Belt, Lean Black Belt, or related certification.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $121,000 to $171,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

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

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.

How this job compares

Set against the 1,055 open Quality Engineering jobs on Olive Jobs, counted November 3, 2026.

Pay
  • This posting$121–171K/yr
  • California median$126–194K/yr113 salary ranges
  • US median$116–181K/yr591 salary ranges

This range's midpoint, $146K, is 10% below the California median midpoint ($163K) — in the middle half of Quality Engineering salary ranges in California.

Openings
Olive Jobs lists 181 open Quality Engineering jobs in California and 1,055 across the US. 7% of them nationwide are listed as remote or flexible.
Hiring the most in California
Experience
This posting asks for at least 5 years of experience; Quality Engineering postings that state a minimum ask for 6 years at the median (766 postings).
Education
451 of the 1,055 open Quality Engineering jobs (43%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 3, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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