Intellectt Inc
QA Specialist
Intellectt Inc, Buffalo Grove, Illinois, United States, 60089
Role:
QA Specialist III
Location:
Buffalo Grove, IL - 60089
Duration:
12 Months
Shift Timings:
8 AM to 4:30 PM
Job Description
Assures the quality of manufactured products and processes per standard operating processes (SOPs) and GMP (Good Manufacturing Practices).Manager Looking For
4 year degree with ~ 5 years experience in a quality function.Quality Experience working in pharma, medical device or related life sciences industry with cGMP / GDP manufacturing environment preferred.Ability to effectively manage smaller projects and day-to-day activities to meet timelines for regular job functions.Supplier Quality Experience with supplier quality metrics, performance monitoring, Supplier CAPA or any combination of the experience is preferred.Skills needed to be successful in position:
Able to use SharePoint cloud-based systems.Knowledge of and previous use of Word tools and Excel.Knowledge of cGMP/ GDP and working in a heavily regulated manufacturing-related environment.Good interpersonal skills to work with individuals from another company to achieve tasks and goals.Ability to complete tasks independently with minimal guidance/oversight.Previous experience in writing CAPA investigations and/or previous experience in managing supplier investigations.Experience in project management is a plus.Regular job functions will be:
Enter records in eQMS systems like Isotrain, Trackwise, Veeva, Agile, SmartSolve, etc.Collect and analyze data for Supplier Metrics.Complete tasks independently with minimal guidance/oversight.Walk the manufacturing and warehouse facility areas for compliance.
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QA Specialist III
Location:
Buffalo Grove, IL - 60089
Duration:
12 Months
Shift Timings:
8 AM to 4:30 PM
Job Description
Assures the quality of manufactured products and processes per standard operating processes (SOPs) and GMP (Good Manufacturing Practices).Manager Looking For
4 year degree with ~ 5 years experience in a quality function.Quality Experience working in pharma, medical device or related life sciences industry with cGMP / GDP manufacturing environment preferred.Ability to effectively manage smaller projects and day-to-day activities to meet timelines for regular job functions.Supplier Quality Experience with supplier quality metrics, performance monitoring, Supplier CAPA or any combination of the experience is preferred.Skills needed to be successful in position:
Able to use SharePoint cloud-based systems.Knowledge of and previous use of Word tools and Excel.Knowledge of cGMP/ GDP and working in a heavily regulated manufacturing-related environment.Good interpersonal skills to work with individuals from another company to achieve tasks and goals.Ability to complete tasks independently with minimal guidance/oversight.Previous experience in writing CAPA investigations and/or previous experience in managing supplier investigations.Experience in project management is a plus.Regular job functions will be:
Enter records in eQMS systems like Isotrain, Trackwise, Veeva, Agile, SmartSolve, etc.Collect and analyze data for Supplier Metrics.Complete tasks independently with minimal guidance/oversight.Walk the manufacturing and warehouse facility areas for compliance.
#J-18808-Ljbffr