Edwards Lifesciences

Edwards Lifesciences

Quality Engineer II - Process Engineering

USA - Utah – Salt Lake City · Mid · Internship

Sponsorship not specifiedDetected 73 days ago
Process ImprovementMedical DevicesCommunicationProblem SolvingCritical Thinking

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odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

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Employer immigration record

from this employer's Department of Labor filings

Green-card follow-through: 50%

Of 10 labor certifications old enough to have been used, 5 expired without the employer filing the next step. Median time from filing to decision: 493 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Files H-1B transfers

3 transfer filings in the last year, covering 3 workers. Median labor-condition decision: 8 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • 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.
  • Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

Requirements

  • Bachelor's degree in engineering or scientific field with two (2) years of Quality Engineering or Manufacturing Engineering experience in a production, manufacturing, or operations environment
  • OR Master's degree in engineering or scientific field with no experience (or applicable internship/co-op experience).
  • Experience supporting production line sustaining activities.

Nice to have

  • Hands-on NCR authoring experience, including investigation, disposition, root cause analysis, corrective action, and documentation closure.
  • Keyence programming experience or experience creating/sustaining optical dimensional inspection routines using similar automated inspection technology.
  • Experience with process validations and test method validations, including protocol execution, report writing, and review of Test Method Validation and OQ/PQ documentation.
  • Experience with FMEAs, risk management documentation, root cause analysis, CAPA support, investigations, and quality improvement initiatives.
  • Working knowledge of quality systems, manufacturing documentation, engineering change control, investigations, and compliance expectations.
  • Strong problem-solving, organizational, analytical, and critical thinking skills with strict attention to detail.

Company info

  • The Quality Engineer II will also be a part of next-generation process development.
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This listing is sourced directly from Edwards Lifesciences's careers page and normalized into a canonical job model.