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Associate i, quality control lab

2 weeks ago


Singapore Alcon MX Full time

Associate I, Quality Control Lab - Chemistry
Associate I, Quality Control Lab - Chemistry
Apply locations Tuas, Singapore time type Full time posted on Posted 3 Days Ago time left to apply End Date: March 31, 2025 (30+ days left to apply) job requisition id R-2025-37526
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 an Associate I, Quality Control Lab
– Chemistry, you are responsible for defining and specifying activities, processes, and standards to fulfill the quality requirements for a manufactured material, component, or product in our Tuas facilities. In this role, a typical day will include:
Responsibilities
Review/Approve testing documentation and test records. Maintain integrity, accuracy and completeness of QC data and records.
Meet quality objectives set by management & comply with Alcon, QMS and Safety requirements.
Timely completion of all compliance activities without overdue, including but not limited to NCI, OOS, CAPA, Effectiveness Check, CR, training, periodic review.
Timely report non-conformance or out-of-specification events. Lead or assist in root cause analyses for product defects and quality lapses, and take effective actions to prevent recurrence.
Drive and promote the continuous improvement culture. Challenge current processes, identify improvements and drive the effort to implement lab system/process while maintaining compliance and reducing human intervention.
Review and assess external standard and/or regulatory requirements pertaining to quality control activities and implement necessary changes to ensure compliance.
Perform basic equipment troubleshooting.
Certified trainer to conduct on-the-job training.
Investigate underlying causes, technical faults and issues pertaining to laboratory equipment, methods or practices, and take necessary actions to resolve the problems.
Develop testing protocols and procedures for Quality Control activities.
Develop APQR sub-reports and ensure timely submission of sub-reports without overdue.
Participate in new product transfer or second sourcing projects and ensure laboratory readiness according to timeline to support the site objectives.
Determine and implement optimal approach for laboratory equipment calibration, maintenance and operation. Ensure laboratory infrastructure and equipment function as intended.
Site point of contact for global communities/initiatives.
Compile data to support business and performance metrics reporting.
Provide guidance, coaching and training to the team as required.
Participate directly in laboratory inspections, internal and external audits.
Analyse data to identify unfavorable trends and address issues with relevant stakeholders to drive improvement on the method robustness.
Perform any other duties as assigned by Supervisor according to business needs.
Perform testing and/or inspection on raw material, in-process material, finished products and monitoring activities.
Perform routine calibration and maintenance of laboratory equipment.
What You'll Bring to Alcon
Bachelor Degree in Chemistry, Bioscience or Microbiology Engineering Related Study.
1-3 years experience in pharmaceutical/medical device industry with GMP knowledge.
Good understanding of the industrial practices and regulatory requirements related to laboratory equipment and computerized systems.
Experience of working in/with QC laboratory. Understand QC requirements and laboratory processes/workflow.
Experience in leading or managing projects.
Experience with managing stability studies, metrology equipment, data analysis or data analytics is an added advantage.
Certified greenbelt is an added advantage.
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.
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