3 of 3 Remote/Hybrid Pharmaceutical Jobs in the Thames Valley

decade of research at UCL, this platform provides a first-of-its-kind biomarker to measure cellular-level changes, supporting global pharmaceutical partners in the fight against blindness and cognitive decline. The Opportunity: As the sole Product Manager, you will have end-to-end accountability for the flagship AI platform. … engineering, and commercial deployment. Own the Trajectory: Lead the product roadmap, balancing regulatory milestones (FDA/ISO) with the requirements of global biotech and pharma stakeholders. Cross-Functional Leadership: Facilitate daily synchronisation between R&D, Data Science, and Clinical verticals to translate complex science into executable work. Technical Authority ...

hours/week £32 p/h About the Role We are seeking a highly organized and detail-oriented System Specialist to support our pharmaceutical manufacturing operations through effective management of the Document Management System (DMS) in preparation to a migration to Veeva Vault system. This role is critical … Cornerstone. • System Optimization and Compliance: Collaborate with QA and IT teams to enhance document workflows and ensure the document management system is optimized for pharmaceutical manufacturing and compliant with regulatory authority requirements (e.g., FDA, EMA), while supporting the Global QMS-DMS team in implementing system improvements, managing technical issues ...

Overview: We’re looking for a detail-oriented System Specialist to manage and support our Document Management System (DMS) within a GMP pharmaceutical environment. This role will focus on document lifecycle management, system coordination, and supporting a migration to Veeva Vault. Key Responsibilities: Manage end-to-end document control (SOPs … across global teams Provide user support, training, and troubleshooting Requirements: Degree in Life Sciences or related field 3+ years in document control within GMP pharma Experience with DMS (D2 or similar systems) Strong knowledge of GMP (e.g., 21 CFR Part 11, EU Annex 11) Excellent organisation and communication skills ...