Quality Documentation Specialist I (Veeva & cGMP)
SGS Consulting
SGS Consulting in Vacaville, CA, seeks a Quality professional to support PQS integration and management of Quality Documents within Veeva. This on-site role requires 1–3 years of Quality experience in pharma or biopharma, preferably in supplier quality. Knowledge of Veeva QDM and strong technical writing skills are a plus. You will collaborate with cross-functional teams to ensure documentation workflows, change control, and regulatory compliance while maintaining readiness for inspections at #J-18808-Ljbffr SGS Consulting
Vacancy posted 3 days ago
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