What are the responsibilities and job description for the Quality Compliance Associate position at SPECTRAFORCE?
Position Title: Quality Specialist I (Quality Compliance Associate)
Work Location: Waukegan Road, North Chicago, IL 60064
Assignment Duration: Through end of year, possible extension based on performance and business need
Work Arrangement: Onsite
Position Summary:
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.
Key Responsibilities:
- 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.
Qualification & Experience:
- Bachelor’s degree, or in progress, preferably in life sciences or engineering
- 0-2 years experience in function or related fields, such as:
- Basic understanding of GLP/cGMP/GCP regulatory standards
- Laboratory and/or Pharma/Device Manufacturing
- Quality Assurance/Regulatory Affairs
- Pharmaceutical/Healthcare Industry
- An 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 required
- Experience Level = 1-3 Years
Mobile-Optimized JD Summary: Entry-level QA Specialist I role onsite in North Chicago, IL. Support supplier audits, admin tasks in pharma R&D. Need basic GxP knowledge, strong comms, computer skills. 10 months, possible extension.
Salary : $25 - $27