Planet Pharma in Maidenhead, UK, seeks a Senior PV Scientist, Quality Document Associate on a 12-month contract. You will review and edit safety documents (PSURs/DSURs) for accuracy, clarity and regulatory compliance, working with PV scientists and report authors on-site.
You should have at least 2 years in quality review/data verification, strong Excel skills, and a background in PV safety or Medical Writing QC. This role offers collaborative teamwork and opportunities to impact patient safety.
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Senior PV Quality Documents Lead (Remote-Eligible) in Maidenhead employer: Planet Pharma
Join a leading biopharmaceutical organisation in Slough, where innovation meets collaboration. As a Scientist in Antibody Formulation Development, you'll thrive in a dynamic work culture that prioritises employee growth and offers unique opportunities to contribute to groundbreaking research. With a focus on professional development and a supportive team environment, this role promises a rewarding experience for those passionate about advancing biopharma solutions.
