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QA Validation & Data Governance specialist at a pharmaceutical manufacturer: reviews validation lifecycle documentation (process, cleaning, equipment, computerized systems), enforces ALCOA+ data integrity in paper and electronic systems, supports deviations/CAPA, and keeps the site inspection-ready. Requires 3-5 years of GMP QA/validation experience and French/English bilingualism.
QA specialist at pharmaceutical manufacturer Jubilant HollisterStier (part of Jubilant Pharma) who oversees validation, qualification, and data-integrity activities to ensure GMP compliance. Day to day involves reviewing validation documentation, supporting computerized-system validation and ALCOA+ data governance, deviations/CAPA, and inspection readiness.
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