Associate QA Specialist

Role: Assist in daily quality operations within a biotech environment, supporting documentation review, audit preparation, and quality metrics tracking. Responsibilities: support CAPAs, Deviations, SCARs, NCRs, maintain training and qualification records, coordinate audit logistics, and assist with document management and system access. Requirements: Associate’s degree or Bachelor’s in Life Sciences or related field; 0–2 years in regulated biotech or similar environment; strong computer skills; good communication, organization, and attention to detail. HighValue: regulatory compliance in FDA, ISO13485, CLIA, CAP; exposure to quality systems, audit support, documentation, and metrics in a biotech setting. WorkSetup: hybrid in San Carlos, CA or Austin, TX; remote within USA; no travel.