31 ago - Milano
Parexel International
Parexel International is seeking an experienced Regulatory Affairs professional to lead regulatory strategy for medical devices and combination products across Europe.
Prima di candidarsi per questo ruolo, la preghiamo di leggere le seguenti informazioni su questa possibilità, riportate di seguito.
You will guide clinical investigations, CE markings, and interactions with health authorities, advising global project teams throughout development and authorization processes.
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We value deep EU MDR knowledge, strong communication skills, and a proven track record in audits and regulatory submissions.
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