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Alcon

Associate II, Quality Operations

Alcon

. Handle complex tasks and contribute to advanced quality management projects within manufacturing and distribution processes .

Posted 10/23/2026full-timeHouston • Texas • United StatesSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in quality management within manufacturing and distribution processes, utilizing problem-solving tools such as 5 Whys and Fishbone Analysis to drive quality outcomes and compliance with GxP regulations.

Highest-signal resume keywords
Quality ManagementRoot Cause AnalysisCorrective And Preventive Action (CAPA)GxP ComplianceData Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Quality MonitoringProblem-Solving Tools5 WhysFishbone AnalysisFMEACAPA DevelopmentQuality Data AnalysisInvestigation DocumentationContinuous ImprovementQuality Records Maintenance
Soft Skills
Independent Decision-MakingCritical ThinkingEffective CommunicationCollaboration
Industry Keywords
ManufacturingDistributionNon-Conformance ResolutionQuality EventsInternal AuditsSOPsRegulatory AffairsQuality System Support

About the role

Key responsibilities & impact
  • Handle complex tasks and contribute to advanced quality management projects within manufacturing and distribution processes
  • Make independent decisions within assigned project areas to drive quality outcomes and operational effectiveness
  • Monitor product quality throughout manufacturing and distribution stages and resolve non-conformances
  • Lead and document investigations related to deviations, non-conformances, and quality events
  • Conduct root cause analyses using 5 Whys, Fishbone Analysis, FMEA, and other problem-solving tools
  • Develop, implement, and monitor corrective and preventive action (CAPA) plans
  • Collaborate with Manufacturing, Quality, Engineering, and Regulatory Affairs teams
  • Communicate investigation status, findings, risks, and scope updates to leadership and stakeholders
  • Prepare and present investigation reports, CAPA summaries, and supporting documentation
  • Maintain quality records and documentation in compliance with GxP regulations and internal procedures
  • Participate in internal and external audits and provide quality system support
  • Analyze quality data and trends to identify continuous improvement opportunities
  • Conduct independent research and apply critical thinking to support quality initiatives
  • Meet individual performance expectations and contribute to organizational quality and compliance objectives

Requirements

What you’ll need
  • Bachelor’s Degree or equivalent years of directly related experience
  • Alternatively, high school diploma plus 8 years of directly related experience
  • Alternatively, associate degree plus 4 years of directly related experience
  • Fluently read, write, understand, and communicate in English
  • Ability to work Monday–Friday, 8:00 AM–5:00 PM CST
  • Ability to work onsite in Houston, Texas
  • 0% travel required
  • Sponsorship and relocation are not available
  • Must comply with GxP regulations, SOPs, training requirements, and applicable industry regulations

Benefits

Comp & perks
  • Health insurance
  • Life insurance
  • Retirement benefits
  • Flexible time off for exempt associates
  • PTO for hourly associates
  • Career growth and development opportunities
  • Reasonable accommodation for individuals with disabilities