Operator I, Quality Operations - 2nd shift

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 Operator I, Quality Operations is primarily responsible for handling manual or operational tasks to ensure efficient quality management processes. You will monitor product quality, resolve non-conformances, and maintain documentation.

• Perform activities that ensure required quality and safety standards are being met for our products.
• Ensure MBR / eMBR reviews are completed promptly based on scheduled due dates.
• Review the MBRs / eMBR to ensure all manufacturing batch procedures are followed, and all data is recorded per procedures.
• Log MBRs / eMBR into a computer tracking system and file pending review.
• Coordinate and support other departments to ensure the smooth execution of work.
• Communicate efficiently with production, maintenance, warehouse, and other functions as necessary.
• Perform housekeeping duties such as keeping work areas clean and free of hazards or dangerous conditions.
• Help support the training needs of team members and work cohesively with team.
• Ensure supplies and equipment are available to meet schedules, and work is carried out as defined by the schedule.
• Adhere closely to Current Good Manufacturing Practices (cGMP), Current Good Documentation Practices (cGDP), and Standard Operating Procedures (SOPs) and report all discrepancies immediately.
• Support facility documentation revision by reviewing documents and processing change requests (review documents, process change requests, temporary document changes, laboratory information system, document obsoletions).

• High School Diploma or equivalent
• The ability to fluently read, write, understand and communicate in English
• 1 Years of Relevant Experience 
• Work Hours: 2nd Shift; Monday – Friday; 2:45pm – 10:45pm CST
• Travel Requirements: None
• Relocation assistance: No
• Sponsorship available: No

• Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
• Collaborate with teammates to share standard processes and findings as work evolves!
• See your career like never before with focused growth and development opportunities!
• Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!

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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 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 alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.