Director, Quality Management Systems

Director Quality Management Systems (QMS)

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 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 Alcons 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 Director Quality Management Systems (QMS) (Management Path) is primarily responsible fordrivingthe developmentimplementation andmaintenance ofQuality Management Systems procedures and activities ensuring regulatory compliance and promoting continuous improvement.This role has significant influence onthe QMS team collaborating with other departments to achieve objectives.

Specificsmayinclude:

• Contribute toleadershipofthe harmonization and standardization of Alcons Quality Management System (QMS) executing departmental strategies that drive compliance efficiency and continuous improvement.

• Partnerwith sites and stakeholders across all organizational levels to ensure alignment of QMS initiatives with company objectives and business priorities.

• Monitor industry trends Health Authority expectations and Notified Body requirements translating emerging standards into business processes quality strategies and organizational capabilities.

• ActivateQuality Information Systems and Training programs ensuring a robust scalable and sustainable quality management framework that supports operational excellence and regulatory compliance.

• Operationalizedepartmental priorities allocate resources and make key decisions regarding budgets projects and strategic initiatives to achieve quality and business objectives.

• Build organizational capability through leadership strategic planning cross-functional collaboration effective communication and development of high-performing teams.

• Drive continuous improvement initiatives that strengthen quality processes enhance operational effectiveness and support a culture of compliance and accountability.

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.