Edwards Lifesciences Corp

Engineer II, Manufacturing, Quality Assurance

Edwards Lifesciences Corp$87K — $123K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or Scientific field required
  • 2 years of hands-on experience in manufacturing or quality roles
  • Preferred experience in the medical device industry
  • Lean Six Sigma Certification advantageous
  • Proficient in engineering methods for process improvement

Responsibilities

  • Lead investigations into quality and compliance issues
  • Drive continuous improvement initiatives using Lean and Six Sigma
  • Partner with teams to manage product and process risks
  • Create and enhance manufacturing documentation and training materials
  • Provide mentorship and technical guidance to technicians
  • Collaborate with teams to implement sustainable quality solutions

Benefits

  • Competitive salaries
  • Performance-based incentives
  • Variety of benefits programs to meet employee needs
Full Job Description

Make a direct impact on product quality and patient outcomes as an Engineer II, Manufacturing Quality Assurance supporting the CAPA team within Irvine Implant Manufacturing. In this role, you'll lead investigations, identify root causes, and drive corrective actions that strengthen quality, compliance, and manufacturing performance.

How you will make an impact:

  • Lead investigations into manufacturing quality and compliance issues, including CAPAs, nonconformances, and audit observations. Perform root cause analysis, develop effective solutions, and drive actions that improve product quality, patient safety, and regulatory compliance.

  • Drive continuous improvement initiatives across manufacturing operations using Lean and Six Sigma methodologies. Identify opportunities to optimize processes, reduce risk, improve efficiency, and enhance overall manufacturing performance.

  • Partner with cross-functional teams to assess and mitigate product and process risks by developing, updating, and maintaining risk management documentation throughout the product lifecycle.

  • Create and improve manufacturing documentation, work instructions, and training materials to support process consistency, operational excellence, and effective knowledge transfer.

  • Provide technical guidance and mentorship to technicians, coordinate testing activities, support execution of engineering projects, and help develop team capabilities through training and coaching.

  • Collaborate with Manufacturing, Quality, and Engineering teams to implement sustainable solutions that strengthen product quality.

What you’ll need:

  • Bachelor's degree in Engineering or Scientific, with 2  years of hands-on experience solving manufacturing or quality challenges, leading investigations, and driving process improvements in a highly regulated environment.

  • Onsite presence is required as this role provides direct support to manufacturing operations.

What else we look for:

  • Medical device industry is preferred.

  • Lean Six Sigma Certification is preferred.

  • Experience with engineering methods (e.g., Six Sigma, LEAN methods, process flow charts, value stream mapping, statistics, and validation) for problem solving, continuous process improvement and sustaining manufacturing support.

  • Understanding statistical and Six Sigma Techniques (Control Charting, DOE, Hypothesis Testing, Gage R&R, Z-Score, Tolerance Analysis, COV, Regression).

  • Demonstrated use of process and design excellence methodologies to optimize processes and Operations Efficiency.

  • Good computer skills in usage of MS Office Suite including MS Project.

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 $87,000 to $123,000 (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.  

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

Similar Jobs

More Jobs at Edwards Lifesciences Corp

More Manufacturing & Automotive Jobs

Find similar Engineer II, Manufacturing, Quality Assurance jobs: