Associate II, Complaints

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, Complaints (Professional Path) is primarily responsible for processing, investigating, and monitoring product defect complaints, serving as the main contact. You will build effective relationships with Medical Safety and Research and Development on adverse events, ensure compliance with regulatory reporting, and provide technical expertise to enhance complaint processing systems.

• Handle complex tasks and contribute to advanced projects in the Complaints discipline
• Process, investigate, and monitor trending and reporting of product defect complaints, ensuring compliance with regulatory agencies' reporting requirements
• Address and expedite product complaints under company policy and procedures
• Make significant decisions within your project area, influencing outcomes
• Support complaint activity monitoring and suggest modifications to 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 following Standard Operating Procedures (SOPs), maintaining accurate documentation, and ensuring quality control
• Complete all required training and meet individual job requirements
• Contribute to the overall compliance and continuous improvement 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.

• Diploma or Bachelor’s Degree in Science, Life Sciences, or Engineering (Open to recent grads)
• Experience in root cause analysis and structured problem solving
• Familiarity with medical devices or pharmaceutical regulations is an advantage
• Ability to communicate effectively in English, both orally and in writing
• Strong communication and problem-solving skills, with the ability to clearly articulate project experience and provide effective responses

• Part of growing company
• Opportunity be involved and exposure to projects from global site

With worldwide headquarters in Atlanta, Ciba Vision is a global leader in the research, development and manufacturing of optical and ophthalmic products and services, including contact lenses and lens care products. Ciba Vision products are available in more than 70 countries worldwide.

With worldwide headquarters in Atlanta, Ciba Vision is a global leader in the research, development and manufacturing of optical and ophthalmic products and services, including contact lenses and lens care products. Ciba Vision products are available in more than 70 countries worldwide.