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Specialist I, Quality Assurance (2nd Shift) - 743999960172055-5844
Specialist I, Quality Assurance (2nd Shift) - 743999960172055-5844-April 2024
Lincolnshire
Apr 1, 2026
About Specialist I, Quality Assurance (2nd Shift) - 743999960172055-5844

  This job was posted by https://illinoisjoblink.illinois.gov : For moreinformation, please see:https://illinoisjoblink.illinois.gov/jobs/11605299 CompanyDescription

  SGS is the global leader and innovator in inspection, verification,testing and certification services. Founded in 1878, SGS is recognizedas the global benchmark in quality and integrity. With over 97,000employees in 130 countries and operating a network of more than 2,400offices and laboratories, we provide services to almost every industryby assuring quality and safety of products and services.

  Job Description

  Specialist I, Quality Assurance is responsible for assisting managementwith the maintenance of the Quality Systems at SGS. The QualityAssurance Specialist must be sensitive to the demanding regulatorycompliance requirements attending to the operation of a pharmaceuticaltesting laboratory. This job also requires the ability to demonstrate ahigh commitment to interpersonal relations.

  Provides support to technical staff in their efforts to ensure thatroutine testing submitted by clients is completed within establishedparameters governing turnaround time, quality specifications, etc.Ensure that all customer requests for information pertaining to SGSservices are met in a timely and effective manner.Issues Certificate of Analysis in a timely mannerReview and approval of method transfer and validation reportsPlay a role in departmental or company wide projects designed toimprove the internal efficiency and overall quality of workperformed at the lab.Participate in creating and maintaining an atmosphere of teamworkthroughout the lab.Provide support in the maintenance of Quality Assurance processes,such as OOS investigations, deviation reporting, vendor approval,internal audits, trending, and other quality systems as directed bymanagementTechnical responsibilities may include reviewing online audit trail,undelete log, computerized system backup activities, assisting inmonitoring list of change controls to ensure timely completion,Project binder, SOP maintenance, and other support activities withinQA and CVS group.Maintain Thorough Knowledge and understanding of all general SOPspertaining to the lab.Maintain thorough knowledge and understanding of GMP/GLP/ISOrequirements as these pertain to work perform in the laboratory.May participate in the preparation and review process of theappropriate department SOPs, worksheets and data formsQualifications

  B.S. in Chemistry, Biology, Microbiology, or related science field

  0-2 years of experience preferably in Life Sciences supporting cGMPOperations

  Thorough knowledge of scientific principles is required

  Monday - Friday 3pm to 11:30pm

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