Quality Assurance Specialist I
On-site · Greenville, South Carolina, United States
Job Summary
Quality Assurance Specialist I is responsible for supporting regulatory-compliant QA activities in pharmaceutical/medical-device manufacturing, including nonconformance management, root-cause analysis, CAPA verification, trend reporting, and QA oversight of validation and documentation. The role requires a life sciences, physical sciences, or engineering degree, familiarity with GMPs and 21 CFR parts 210/211/820, ISO 13485, and potential CQA/CQE/CQM certifications; candidate should be detail-oriented, organized, and capable of supporting continual quality improvements across product life-cycle stages.
Required Qualifications
- Bachelor’s degree (BA/BS) in life sciences, physical sciences, engineering, or a related field is required
Additional Requirements
- Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
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