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- ...other stakeholders on the development, evaluation and surveillance of human medicines. •Be responsible for outcome and opinion documents for pre- and post-authorisation procedures, ensuring high-quality EPARs and product information for the assigned portfolio. Working...ZasugerowanePełny etatElastyczne godziny
European Medicines Agency
Holandia18 dni temu - ...contact for internal and external audits Provide evidence, documentation, and walkthroughs for auditors Track audit findings and support remediation efforts Reporting & Documentation Document control testing results, findings, and risk implications Produce...ZasugerowanePraca z domuElastyczne godziny
