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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Intake Quality Lead for Global Adverse Events in Maidenhead employer: Biopharma Careers
Boehringer Ingelheim UK is an exceptional employer that fosters a collaborative and innovative work culture, providing employees with the opportunity to grow professionally within the dynamic pharmaceutical industry. With a strong emphasis on employee development and well-being, the company offers comprehensive benefits and a supportive environment that encourages meaningful contributions to healthcare advancements.
