A mid-sized biotechnology company in Maidenhead is seeking a PV Scientist Quality Document Manager to manage the quality of safety surveillance documents. This role requires a keen eye for detail to ensure compliance with stringent quality standards. You will collaborate with diverse stakeholders to enhance pharmacovigilance documentation. Strong organizational and writing skills, along with a Bachelor's degree in a relevant field, are essential. This position allows for hybrid work, requiring 50% weekly attendance in the office.
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