Senior Quality Engineer II

Senior Quality Engineer IIAt 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 Senior Quality Engineer II you are tasked to drive and assist on daily operations (Vision Care and Surgical), including validation/qualification activity, continuous improvement, failure investigation & root cause analysis of GMP issues in the manufacturing at Batam. In this role, a typical day will include:Responsibilities:Responsible to assist and support Failure Investigation and root cause analysis.Act as QE SME for Validation/QualificationResponsible to manage & support validation/qualification activities for product/process/system/equipment and raw material of Alcon products.Responsible to ensure compliance and provide guidance and technical support to Quality/Production function.Responsible to perform product/process/system risk/impact assessment and provide the vision from quality point of view on risk/impact management review and approval (as applicable).Responsible to lead and drive Quality Improvement and support Continuous Improvement Initiatives (CII) for Vision Care and Surgical Products.What Can You Bring to Alcon:Minimum Degree in Science/Engineering or related studies.5+ Years of Experience in Pharmaceutical / Medical Device Industry preferredWhy 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.Drive and assist on daily operations (Vision Care and Surgical), including validation/qualification activity, continuous improvement, failure investigation & root cause analysis of GMP issues in the manufacturing