24/04/2024 | Fulltime | Mildenhall | CV-LibraryCFR part 21, MDR and other medical device regulatory requirements. - Generate documentation in line with ISO 9001 requirements and other non-medical regulatory requirements. - Perform tooling, equipment, system and manufacturing validation qualification for both medica and non-medical products. - Lead
Save for laterRegister your CV19/02/2024 | Fulltime | Mildenhall | 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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