Associate I, Quality Control Labs (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 Associate I, Quality Control Labs (Para-Professional & Support Path), is primarily responsible for performing business support tasks in the Quality Control Labs, including inspection, testing, and analysis of products and raw materials. You will report test results accurately and work with cross-functional teams to ensure seamless integration of lab results.

Specifics Include:

• Perform business support or clerical tasks in the Quality Control Labs according to procedures, contributing to efficient business operations through accurate task completion
• Follow established procedures with limited decision-making authority, requiring job-related training, attention to detail, and reliability
• Conduct inspection, testing, and analysis of products and raw materials to ensure they meet required specifications and standards, utilizing various analytical techniques and lab equipment
• Report test results accurately and collaborate with cross-functional teams, including production, engineering, and quality assurance, to ensure the seamless integration of lab results into the manufacturing process
• 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
• Commit to continuous improvement and compliance with regulatory requirements, meeting individual job requirements and contributing to the overall compliance of the organization. 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​.