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Salary
$66k – $151k per year (Estimated)
Location
In office (Houston)
Seniority
Middle · 8+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Alcon is a Swiss eye care company founded in Texas in 1945 that was owned by Nestle and then Novartis before being spun out as an independent listed company in 2019. It operates in two halves: surgical, which supplies the intraocular lenses, phacoemulsification equipment and consumables used in cataract and vitreoretinal surgery, and vision care, which sells contact lenses and eye drops. Headquartered in Geneva and listed in Zurich and New York, it is the largest eye care device company in the world and benefits directly from ageing populations, since cataract surgery is among the most common procedures performed anywhere.

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. 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. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.

The Associate II, Quality Operations (Professional Path) is primarily responsible for managing complex quality processes, leading investigations, and contributing to advanced quality management initiatives. This role supports product quality monitoring, non-conformance resolution, CAPA management, compliance activities, and continuous improvement efforts across manufacturing and distribution operations while applying advanced quality systems knowledge.

Specifics Include:

  • 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 various stages of manufacturing and distribution and ensure timely resolution of non-conformances

  • Lead and document investigations related to deviations, non-conformances, and quality events in accordance with established procedures

  • Conduct thorough root cause analyses utilizing appropriate methodologies such as 5 Whys, Fishbone Analysis, FMEA, and other problem-solving tools

  • Develop, implement, and monitor corrective and preventive action (CAPA) plans to mitigate risk, prevent recurrence, and improve process performance

  • Collaborate cross-functionally with Manufacturing, Quality, Engineering, and Regulatory Affairs teams to ensure effective investigations and sustainable CAPA implementation

  • Communicate investigation status, findings, risks, and scope updates to leadership and key stakeholders

  • Prepare and present investigation reports, CAPA summaries, and supporting documentation for management reviews and regulatory inspections

  • Maintain accurate quality records and documentation in compliance with Good Practice (GxP) regulations and internal procedures

  • Ensure adherence to Standard Operating Procedures (SOPs), training requirements, and applicable industry regulations

  • Participate in internal and external audits, providing quality system support, CAPA documentation, and responses as required

  • Analyze quality data and trends to identify opportunities for continuous improvement and enhanced process performance

  • Conduct independent research and apply critical thinking to support quality initiatives and optimize business outcomes

  • Meet individual performance expectations while contributing to organizational quality and compliance objectives

WHAT YOU’LL BRING TO ALCON:

  • Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)

  • The ability to fluently read, write, understand, and communicate in English

  • Work Hours: Monday - Friday: 8:00 AM CST - 5:00 PM CST

  • Travel Requirements: 0%

  • Location: Onsite

  • Sponsorship & Relocation: Not Available

HOW YOU CAN THRIVE AT ALCON:

  • Collaborate with teammates to share standard processes and learnings as work evolves!

  • 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!

  • Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!

Alcon Careers

See your impact at alcon.com/careers

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.

Find Jobs for Employees

Find Jobs for Contingent Worker

ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY

Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [email protected] and let us know the nature of your request and your contact information.

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