Edwards Lifesciences Corp

Senior Quality Engineer, Metals Process Engineering

Edwards Lifesciences Corp$90K — $120K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Master's degree in Engineering or related scientific field with applicable experience.
  • 4+ years of relevant experience (Bachelor's) or 3+ years (Master's) in quality engineering or related roles.
  • Experience with manufacturing of metal implants and precision devices.
  • Familiarity with New Product Development (NPD) and New Product Introduction (NPI) processes.
  • Expertise in statistical techniques and control methodologies such as Six Sigma.

Responsibilities

  • Lead development and optimization of testing methods for nitinol frames and components.
  • Implement advanced process monitoring and statistical control to enhance manufacturing stability.
  • Drive complex experimental validation processes, collaborating with cross-functional teams.
  • Select and validate engineering equipment to meet production requirements.
  • Provide mentorship and training for effective knowledge transfer to global teams.
  • Create risk management documentation with engineers to address manufacturing challenges.
  • Investigate and resolve product quality issues, making data-driven recommendations.

Benefits

  • Comprehensive health and wellness programs.
  • Opportunity for professional development and further education.
  • Flexible work arrangements for work-life balance.
  • Access to modern engineering tools and techniques.
  • Collaborative working environment across multiple international sites.
Full Job Description
As a Senior Quality Engineer within the Metals Process Engineering Group (MPEG), you will support nitinol frame and implant component development. This role will support multiple phases of nitinol product(s) development projects such as design verification, validations, launch and stabilize, and transfers to Ireland and Singapore. As the Quality engineer, you will support advanced characterization, functional testing, and inspection development. You will also provide advanced understanding of the product development process, risk management, process monitoring and control, validations, traceability and risk-based decision making.

How You'll Make an Impact:

  • Support or lead identification, development, and optimization of complex material characterization, testing methods, and inspection processes using engineering methods (e.g., Six Sigma and Lean manufacturing tools) for development of nitinol frame and component processes.
  • Implement advance process monitoring and statistical process control of complex processes to drive process control, capability and stability.
  • Drive the development and manage the execution of complex experiments and tests (including writing and executing protocols) to validate and improve products (including evaluation of source materials and suppliers) and establish robust manufacturing processes/test methods based on engineering principles; ensure completion of comprehensive process validations (TMV/IQ/OQ/PQ), including analyzing results and developing reports; collaborate with cross-functional team members to facilitate project success and on-time completion.
  • Collaborate with engineers for equipment selection and validation.
  • Provide training and mentorship to enable the seamless knowledge transfer of project and manufacturing processes to receiving sites (Draper, Ireland, Singapore)
  • Develop technical content of risk management documentation and partner with DA and R&D engineers to ensure nitinol manufacturing considerations are incorporated into RMW, FMEAs, QCPs, etc.
  • Lead in the investigation of complex manufacturing product quality and compliance issues (e.g., Material Review Board, SCAR, CAPA, non-conformances, audit observations) based on engineering principles; analyze results, make recommendations and develop reports.
  • Train, coach, and guide other quality engineers on complex principles
  • Oversee Quality support tasks; gives instruction to engineers/technicians on conducting tests; trains engineers/ technicians and provides feedback; and may coordinate engineers/ technician work.
  • Review and approve compliant change control.
  • Other incidental duties


What You'll Need (Required):

  • Bachelor's degree in Engineering or a scientific field with 4 years of relevant experience, or Master's degree in Engineering or a scientific field with 3 years of relevant experience.


What Else We Look For (Preferred):

  • Experience with manufacturing of metal implants, frames, stents, valves, delivery system components, or other precision implantable devices.
  • Experience supporting NPD/NPI programs, along with design verification, design validation, process validation, and product launch activities.
  • Supporting design transfer and manufacturing transfers.
  • Developing inspection strategies and test methods for implantable products.
  • Experience with pFMEA, dFMEA, process characterization, and process controls.
  • Experience using risk-based decision making throughout the product lifecycle.
  • Leading IQ/OQ/PQ and process validation activities.
  • Proven expertise in statistical techniques and SPC
  • Experience with automation, software testing, and software validation is strongly preferred
  • Proven expertise in usage of MS Office Suite
  • Ability to read and interpret drawings
  • Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills
  • Ability to translate technical information to all levels of the organizations
  • Knowledge of Six Sigma concepts with ability to apply to work product
  • Knowledge of Quality Engineering concepts with ability to apply to work product
  • Strong leadership skills and ability to influence change

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

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