Senior Validation Engineer

Role: Support validation and qualification activities within Alcon's engineering team to ensure equipment, systems, and processes meet regulatory and quality standards. Responsibilities: plan, execute, and document validation studies; review change controls; support aseptic process validation; author validation protocols and reports; conduct risk assessments; oversee process qualification for new technologies; participate in transfers and launches; ensure compliance with GxP regulations; collaborate with cross-functional teams for problem-solving and continuous improvement. Requirements: Bachelor’s degree or equivalent with 2+ years of relevant experience; proficiency in validation, change control, deviation investigation, and data analysis; familiarity with sterilization methods and thermal validation preferred. High-Value: validation in regulated pharmaceutical or biologics manufacturing, aseptic processes, sterilization validation, GxP compliance, and working within quality management systems. Work setup: exempt role with no travel requirements; position may be at Associate I or II level based on experience.