Alcon Research

Alcon Research

Principal II, Research & Development Quality Assurance

Fort Worth, Texas · Principal · Contract

Sponsorship not specifiedDetected 76 days ago
FDA RegulatoryMedical DevicesResearchGxPRegulatory Affairs

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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.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Green-card follow-through: 44%

Of 9 labor certifications old enough to have been used, 5 expired without the employer filing the next step. Median time from filing to decision: 478 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.

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

  • With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health.
  • We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before.
  • ATTENTION: Current Alcon Employee/Contingent Worker If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Responsibilities

  • Operates with independence from business partners to provide oversight of quality and compliance operations
  • Manage individual technical projects, applying specialized knowledge to achieve objectives and drive innovation.
  • Lead the resolution of individual deviations and Corrective and Preventive Actions.

Requirements

  • Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training.

Nice to have

  • Certified Quality Engineer (CQE) or other relevant ASQ certification
  • Knowledge of FDA 21 CFR Part 820, ISO 13485, and ISO 14971
  • Knowledge of CAPA, Nonconformance Management, and Root Cause Analysis
  • See your career like never before with focused growth and development opportunities
  • Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
  • Familiarity with EU MDR, MDSAP, and global regulatory requirements

Benefits

  • Assure successful development, documentation, quality control, validation, and transfer of high-quality and reliable medical devices.

Company info

  • At Alcon, we're passionate about enhancing sight and helping people see brilliantly.

Visa & Work Authorization

  • Sponsorship Assistance: No

This listing is sourced directly from Alcon Research's careers page and normalized into a canonical job model.