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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in supplier management, quality assurance methodologies, and compliance with regulatory standards. Proven ability to lead cross-functional teams, mentor personnel, and drive continuous improvement initiatives within the medical device industry.
Highest-signal resume keywords
Supplier ManagementQuality Assurance MethodologiesRegulatory ComplianceLeadership ExperienceSupplier Audits
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Supplier EvaluationRisk Minimization StrategiesCorrective and Preventive Actions (CAPAs)Continuous Improvement InitiativesCompliance Assessments
Soft Skills
MentoringCross-Functional CollaborationCommunication
Tools & Technologies
Alcon Quality SystemGxP RegulationsSOPs
Industry Keywords
Medical Device IndustryRegulated IndustrySupplier Performance Monitoring
About the role
Key responsibilities & impact- Lead the supplier management program across Alcon’s global network
- Evaluate, qualify, assess capability, and monitor supplier performance
- Champion continuous improvement initiatives and ensure uninterrupted supply of high-quality components
- Develop strategies to mitigate manufacturing issues at facilities in Lake Forest, CA, Fort Worth, TX, or Johns Creek, GA
- Develop and execute pre-market supplier selection, evaluation, and risk-minimization strategies
- Oversee multiple projects and supervise work to ensure goals are met
- Supervise supplier Corrective and Preventive Actions (CAPAs)
- Facilitate global supplier performance monitoring and report to senior and executive management
- Mentor supplier quality personnel
- Lead cross-functional meetings for supplier performance monitoring and issue resolution
- Develop and improve procedures, policies, and quality assurance methodologies
- Monitor adherence to Alcon Quality System requirements and regulatory standards
- Perform compliance assessments and supplier and contract-manufacturer audits globally
- Develop and execute supplier selection, evaluation, and compliance strategies
- Partner with Global Sourcing and Procurement, Regulatory, Operations, and Quality teams
- Manage resources and schedules for supplier audits and quality initiatives
- Follow GxP regulations, SOPs, documentation, and required training
- Contribute to organizational compliance and continuous improvement
Requirements
What you’ll need- Bachelor’s Degree or equivalent years of directly related experience (or high school +15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs)
- Fluency in reading, writing, understanding, and communicating in English U.S.
- 7 Years of Relevant Experience
- 5 Years of Demonstrated Leadership
- Preferred: Medical Device industry or other regulated industry experience
- Ability to work Monday–Friday, 8:00 AM–5:00 PM CST
- Up to 10% travel
- Sponsorship is not available
Benefits
Comp & perks- Relocation assistance
- Health benefits
- Life insurance
- Retirement benefits
- Flexible time off for salaried associates
- Paid time off for hourly associates
- Programs promoting health and well-being
- Financial security programs
- Retirement planning support
- Short-term and long-term incentive opportunities for eligible roles