Associate II, Quality Operations

Role: Associate II, Quality Operations (Professional Path) at Alcon, focusing on managing complex quality processes within manufacturing and distribution to ensure product compliance and quality standards. Responsibilities include leading investigations of deviations/non-conformances, performing root cause analyses using methodologies like 5 Whys and FMEA, developing and implementing CAPA plans, monitoring product quality across production stages, and supporting regulatory and audit activities. Requirements: Bachelor's degree or equivalent experience (e.g., 8+ years high school + work in quality), proficiency in English, onsite work, no travel requirement, Monday–Friday schedule. High-Value: biopharma quality management, manufacturing and distribution oversight, deviation investigation, root cause analysis, CAPA development, GxP compliance, audit support, continuous improvement initiatives. Collaboration with Manufacturing, Quality, Engineering, and Regulatory teams is essential. Location: Onsite in a drug/device manufacturing environment; no travel specified.