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 Technician III, Quality Control Labs (Science/Tech/Engineering Path), is primarily responsible for handling complex technical tasks in Quality Control Labs, including inspection, testing, and analysis of products and raw materials. You will be expected to make significant decisions and build effective relationships with cross-functional teams.

Specifics Include:
• Handle highly complex technical tasks, supporting operations and contributing to efficiency within defined procedures
• Perform inspection, testing, and analysis of products and raw materials to ensure they meet required specifications and standards
• Utilize various analytical techniques and handle lab equipment, reporting test results
• Make significant decisions within the scope of tasks, requiring advanced technical skills and problem-solving abilities
• Support lab operations and collaborate with cross-functional teams, including production, engineering, and quality assurance, integrating lab results into the manufacturing process to drive problem-solving and innovation through scientific principles
• Adhere to Good Practice (GxP) regulations by strictly following Standard Operating Procedures (SOPs) and maintaining accurate and complete documentation to ensure rigorous quality control
• Complete all required training and meet individual job requirements, contributing to the overall compliance of the organization
• Commit to continuous improvement and compliance with regulatory requirementsAll 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​.

Qualifications:

• Education: Minimum Diploma (D3), preferably in Engineering or another relevant technical/science discipline.
• Experience: 1–2 years of experience in Quality Control, Incoming Inspection, Manufacturing, or the Medical Device industry is preferred. Fresh graduates are welcome to apply.
• Technical Knowledge: Able to read and understand technical drawings, specifications, and inspection requirements. Basic knowledge of GD&T according to ASME Y14.5 and the ability to interpret engineering drawings are preferred.
• Computer Skills: Basic proficiency in Microsoft Office applications.
• Language: Able to communicate in English and understand written English used in technical specifications, procedures, and work instructions.

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