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QC Lab Final Inspection & Micro QC Manager

Alcon Research


Job Location:

Johns Creek, GA - USA

Monthly Salary: Not provided by the employer
Posted: 17 May 2026 (30+ days ago)
Application Deadline: 14 August 2026
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

Job Summary

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 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 Alcons 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 QC Lab Final Inspection & Micro Quality Control Manager is responsible for the overall operation compliance and performance of assigned Quality Control laboratory functions. This role provides operational technical and people leadership for Final Inspection and Microbiology laboratories while partnering crossfunctionally to ensure regulatory compliance product quality and operational excellence.

Specifics Include:

  • Lead and oversee daily operations performance and compliance of Final Inspection and Microbiology Quality Control laboratories

  • Manage Quality Control activities related to inspection testing and analysis of finished products and inprocess materials to ensure conformance to approved specifications and standards

  • Oversee metrology and final lens inspection testing for finished contact lens products

  • Manage microbiology laboratory operations including environmental and water monitoring bioburden testing growth promotion compressed air and nitrogen testing

  • Ensure laboratory readiness through proper inventory control of equipment consumables reagents standards and chemicals

  • Ensure all laboratory testing and inspections comply with SOPs cGxP requirements and regulatory expectations

  • Review interpret and evaluate analytical and microbiological data for accuracy precision and adherence to specifications

  • Identify quality trends investigate deviations and drive corrective and preventive actions to mitigate ongoing or potential production issues

  • Manage instrument and equipment qualification calibration coordination and method validation activities

  • Partner with AS&T to onboard qualify and validate new laboratory equipment and technologies

  • Collaborate closely with MDLIMS to continuously improve master data test methods and workflows aligned with laboratory operations

  • Support hiring onboarding training and ongoing development of laboratory associates

  • Ensure personnel proficiency in laboratory techniques equipment use documentation and data integrity practices

  • Oversee departmental training programs including training plans handson instruction compliance tracking retraining and development of new training modules

  • Foster a culture of quality accountability safety engagement and continuous improvement

  • Provide quality and technical support to Manufacturing to ensure product quality compliance and uninterrupted operations

  • Lead and support continuous improvement initiatives related to quality efficiency compliance and new product or process introductions

  • Prepare and present laboratory performance metrics quality trends and compliance with data to internal and external stakeholders

  • Ensure department safety requirements are consistently met including chemical storage hazard communication equipment maintenance and resolution of employee concerns

  • Lead laboratory tours and support internal customer and regulatory inspections and audits

  • Develop and manage the annual laboratory operating budget and departmental inventories

  • Maintain full compliance with all applicable GxP regulations by following established procedures maintaining accurate documentation and completing all required training

WHAT YOULL BRING TO ALCON:

  • Bachelors Degree or Equivalent years of directly related experience (or high school 13 yrs; Assoc.9 yrs; M.S.2 yrs; PhD0 yrs)

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

  • 5 Years of Relevant Experience

  • Work hours: 1st Shift: Monday Friday: 8:00 AM EST 5:00 PM EST

  • Travel Requirements: 0%

  • Location: Onsite

  • Sponsorship & Relocation: Not Available

PREFERRED QUALIFICATIONS/SKILLS/EXPERIENCE:

  • Experience leading both Microbiology and Final Inspection Quality Control laboratories

  • Strong working knowledge of cGxP data integrity principles and regulatory inspection readiness

  • Experience using laboratory information management systems (e.g. MDLIMS)

  • Demonstrated experience supporting internal customer and regulatory audits

HOW TO 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 Alcons 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:

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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.

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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 and let us know the nature of your request and your contact information.


Required Experience:

Manager


About Company

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Our mission is to provide innovative vision products that enhance quality of life by helping people see better. From vision research to eye health, learn more at Alcon.com.

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