Intake Quality Lead for Global Adverse Events

CSL Seqirus based in Maidenhead, UK, is seeking a dedicated professional to govern the intake of adverse event reports. You will ensure vendor performance aligns with CSL PV processes, provide training, and lead cross-functional documentation and CAPA readiness.

The role requires strong pharmacovigilance expertise, knowledge of MedDRA/WHO-DD, and experience with regulatory inspections. Hybrid work profile: 3 days on site in Maidenhead.

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