Latest Drug Regulatory Affairs jobs in Reading - JobisJob United Kingdom Mobile

7 Drug Regulatory Affairs Jobs in Reading

Regulatory Affairs Manager CK Group- Science, Clinical and Technical - Uxbridge, United Kingdom Act as a contact with relevant regulatory agencies in fulfilling local obligations by product assignment and document and communicate details and outcomes of regulatory agency interactions to senior management... £0 - £45.56/hour 14 days ago
Manager, Regulatory Affairs-hybrid role abingdon, england, United Kingdom Preparation of regulatory submissions including: INDs, CTAs, GMOs, IDEs, amendments, annual reports, meeting briefing documents, responses to regulatory agency information requests, marketing authorization... 14 days ago
Associate Director, Quality Control Oxford, England, United Kingdom Gain a comprehensive understanding of Moderna's Quality Control processes and standards, specifically focusing on the nuances of commercial testing functions for mRNA products. This includes familiarization... 13 days ago
Director - Real-World Evidence (Observational Research Operations) Uxbridge, England, United Kingdom Leveraging strong organization skills and clinical research operations background, the RWE Observational Research Operations Director plays an integral part in audit readiness through operational management... 16 days ago
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Regulatory CMC Scientist - Small Molecule slough, england, United Kingdom Many years of relevant experience including a broad background of registration experience gained from working in the pharmaceutical industry, preferably in Regulatory Affairs CMC and/or in pharmaceutical... More than 30 days ago
QA Specialist slough, england, United Kingdom Stay abreast with GCP, GLP, regulatory, and industry trends. Share key information gathered via professional associations and conferences (upcoming regulations, best practices) within the GCSO Practice... More than 30 days ago
Manager, Regulatory Affairs-hybrid role abingdon, england, United Kingdom Preparation of regulatory submissions including: INDs, CTAs, GMOs, IDEs, amendments, annual reports, meeting briefing documents, responses to regulatory agency information requests, marketing authorization... More than 30 days ago

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