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, Complaints is primarily responsible for processing and investigating complaints, ensuring compliance with regulatory requirements, and supporting project goals. Job responsibilities: • Apply specialized knowledge to perform tasks and achieve objectives in the Complaints discipline • Process, investigate, and monitor trending and reporting of product defect complaints, serving as the primary contact • Align with Medical Safety and/or Research and Development on adverse events • Address and expedite product complaints under the company's complaint policy and procedures • Ensure compliance with regulatory agencies' reporting requirements • Follow procedures with some decision-making authority, requiring job-related training, attention to detail, and reliability • Support complaint activity monitoring and provide suggestions to modify existing manufacturing or packaging processes • Maintain unified product defect investigation operating procedures • Collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles • Adhere to Good Practice (GxP) regulations by strictly following Standard Operating Procedures (SOPs) • Maintain accurate and complete documentation and ensure rigorous quality control • Complete all required training and meet individual job requirements to contribute to the overall compliance of the organization • Commit to continuous improvement in operationsAll 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. Minimum requirement: Min Bachelors Degree in Science or Engineering, chemistry related Preferable min 1-2 years experience in Lab testing. General working hours 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 At Alcon, we are committed to helping people see better. We believe patients should have access to quality eye care regardless of their economic circumstances; however, barriers to good eye health exist for patients in both developed and emerging markets. Alcon develops and manufactures innovative devices to serve the full life cycle of eye care needs. Its surgical group is one of the largest makers of equipment used for cataract removal and laser vision correction. Its consumer products include the well-known Opti-Free line of contact lens solutions and related products. Alcon, which was founded in 1945, sells its products in 180 countries worldwide. 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