New 
Quality Assurance (QA) Specialist I
 Spectraforce Technologies | |
 United States, Illinois, North Chicago | |
 Jan 28, 2026 | |
| The Abbvie Sponsor is Michael OrrJob Description:Primarily responsible for carrying out basic tasks related to core job responsibilities under the supervision/oversight from their direct manager and/or designee. This is an entry-level quality assurance position. The incumbent is in a skills learning mode; supervisory review and oversight is expected; however, the incumbent is expected to demonstrate some decision-making ability under the supervision of management. Limits to freedom and individual action by the incumbent are based on the level of expertise and interpersonal skills possessed. The incumbent may interact with employees, managers, and cross-functional peers. They may also represent functional area on cross-matrixed project teams with other functional leaders.Carryout job duties under guidance of management and/or designee, including the planning and scheduling of third-party supplier audits.Support the planning and conduct of paper-based quality assessments of third-party suppliers (e.g. Quality Questionnaires, Quality History).Support the maintaining of approved supplier list, global audit schedule, and participate in supplier management processes.Gathers internal and external audit metrics and presents to QA management for trend analysis.Assist External Partners Quality management on the collaboration with Inspection Management group on external party audits by regulatory agencies or customers.Assist senior auditors and management to develop, maintain and update departmental systems, procedures, and records pertinent to position responsibilities.Expected to elevate any issues to management, as necessary, in meeting these responsibilities.Support group goals, with possibility of leading departmental level goals. Resolves project team issues with minimal oversight.Prepare and present project progress reports to update management and keep the team(s) informed.Qualifications:Bachelor's degree, or in progress, preferably in life sciences or engineering0-2 years experience in function or related fields, such as:Basic understanding of GLP/cGMP/GCP regulatory standardsLaboratory and/or Pharma/Device ManufacturingQuality Assurance/Regulatory AffairsPharmaceutical/Healthcare IndustryAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Assures the quality of manufactured products and processes per standard operating processes(SOP'S) and GMP (Good Manufacturing Practices). Degree not requiredExperience Level = 1-3 Years Enable Skills-Based Hiring No Provide the days of the week and the hours that this position will require: (No Value) | |