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Posted today by Arevna
Maintenance of other technical documentation to ensure compliance to 21 CFR 820, ISO 13485 and MDR 2017/745 including. o Design History File / Design and Development File. o Device Master Record / Medical Device File. o Technical Files. Participate in engineering change requests as part of … more
Posted 2 weeks ago by Calibre8 Recruitment Ltd
Graduate Trainee - Medical Device Sales. Outline. This is fantastic opportunity for someone who would like to start a career in Medical Device Sales. Ideal for a graduate of Human Sciences or a clinical person who wants to progress away from direct care. The Company. An … more
