Alcon is seeking an Associate I, Regulatory Operations to support the Quality & Regulatory Affairs function. The role involves handling regulatory submissions, maintaining databases, preparing dossiers, managing compliance with global regulations, and ensuring product quality standards. The position requires specialized knowledge in regulatory operations, attention to detail, and adherence to Good Practice (GxP) regulations.
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.
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. The Associate I, Regulatory Operations is primarily responsible for supporting project goals by handling regulatory submissions, maintaining databases, and ensuring compliance with external regulations.
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. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.
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