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 Assurance Compliance , is primarily responsible for handling complex tasks in Quality Assurance Compliance, ensuring quality control practices are implemented, and managing Quality Systems, Complaints, and Supplier Quality Management processes at our Manufacturing location in Houston, TX. In this role, a typical day will include: Handle complex tasks and contribute to advanced projects in Quality Assurance compliance Ensure effective implementation of quality control practices and principles Manage Quality Systems Management, Complaints Management, and Supplier Quality Management processes Ensure compliance with current Good Manufacturing Practices (cGMP), Health Authority, Alcon Quality Manual requirements, and International Organization for Standardization (ISO) standards Make significant decisions within project areas, influencing outcomes Facilitate the implementation of the Quality Strategy and support governance processes Conduct audits and advise on policy Collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, and ensuring rigorous quality control Complete all required training and meet individual job requirements Contribute to the overall compliance of the organization by committing to continuous improvement and regulatory compliance All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees