Genovice INC
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Agency • Healthtech • Professional Services • Biotech
Leads quality-system development and computerized system validation governance for a regulated technology company. Responsibilities include building the QMS, authoring SOPs, overseeing document and change controls, CAPA, deviations, training, supplier quality, audits, validation reviews, data-integrity controls, inspection readiness, and regulated product-release approvals. The role provides independent Quality oversight rather than executing routine testing and requires approximately 20 hours per week.
