21/03/2024 | Fulltime | | United Kingdom | CV-Library | €59,000 / Year Of stability, process validation and analytical method validation protocols. - Manage and monitor the progress of validation activities (analytical and manufacturing process) and stability studies, highlighting any out of specification/trend results. - Review batch documentation updates for existing commercial
Save for later21/03/2024 | Fulltime | | United Kingdom | CV-Library | €59,000 / Year Of stability, process validation and analytical method validation protocols. - Manage and monitor the progress of validation activities (analytical and manufacturing process) and stability studies, highlighting any out of specification/trend results. - Review batch documentation updates for existing commercial
Save for later19/02/2024 | Fulltime | | United Kingdom | CV-LibraryWith ISO13485 and other medical device regulatory requirements. - Leading, running and moderating use studies such as formative and summative evaluations. - Work closely with the customers and clinical experts to gather relevant information. - Work closely with the project and wider teams to create a device
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