A leading biotechnology company in Maidenhead is seeking a PV Scientist Quality Document Manager to ensure high-quality standards in Safety Surveillance documentation. The role involves verifying data accuracy, conducting editorial reviews, and collaborating with stakeholders to drive quality process improvements. Ideal candidates have a Bachelor’s in a relevant field, experience in pharmacovigilance or medical writing, and strong organizational skills. This hybrid role requires 50% weekly office attendance in Maidenhead.
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