Quality Assurance Specialist

Spectraforce Technologies
United States, Illinois, North Chicago
Nov 08, 2024
Title: QA Specialist I Duration: 1 year Location/Site: North Chicago, IL Purpose: Perform sampling, inspecting, and physical testing of incoming commodities per appropriate product specifications in a laboratory. Environment. Applies scientific knowledge to daily operations, data management, and problem-solving. Understands and Follows documentation. Analyzes basic/simple data, evaluates results, forms conclusions, and recommends Process and document improvements. Recognizes deviation from normal operating procedures. Recognizes And troubleshoots instrumentation and work order problems and routine operational issues. Responsibilities: Responsible for performing routine testing on incoming materials by approved specifications and procedures. Disposition of incoming material for use in manufacturing. Maintains certification in assigned job responsibilities and completes training on time. Participates in complaint handling, failure investigations, and CAPA documentation. Understands, implements, and maintains the quality policy and ensures compliance with level policies and Procedures. Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external Support groups to perform core skills. Participates in team activities and area metric tracking. Responsible for supporting Operations efforts in meeting established production schedules. Reports problems in a timely and accurate manner. Seeks additional guidance or advice when the problem is beyond the scope of training or knowledge. Qualifications: High School Diploma required, Bachelor's degree preferred. Good understanding of basic math. Good clerical skills are required. 4+ years of overall work experience Computer skills proficiency including word processing, spreadsheets, instrumentation related, and Client Network systems. Previous experience in Quality Assurance 2+ Experience in a manufacturing/finishing environment is desired. Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired. Have an understanding of material/product traceability and Device History Records.