At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
As a Quality System Intern, you are to be responsible for the site's document control and records management for compliance to ISO 13485, MDSAP, EU MDR and, Alcon Standards and Policies in our Tuas Site. In this role, a typical day will include:
· Perform archival of electronic documents, based on retention period requirements.
· Identify improvement opportunities and lead/support the implementation activities to improve performance and efficiency
· Ensure no backlog of record archives for electronic documents
· Assist in the migration of new quality system Box (from Alfresco)
· Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements
· Work with cross-functional teams to resolve operational quality issues
· Performs any other duties as assigned by Supervisor according to business needs
· Adhere to Alcon standards, in particular quality, ethical, health, safety and environment (HSE) and information security (ISEC) standards
· Complete project above as per stipulated timeline
What You'll Bring To Alcon
· Undergraduates Diploma/Degree in Engineering
Why Join Us:
• Opportunity to work with a leading global medical device company.
• Collaborate with a diverse and talented team in a supportive work environment.
• Competitive compensation package and comprehensive benefits.
• Continuous learning and development opportunities.
