| http://www.w3.org/ns/prov#value | - ll products and processes and project tasksTypically this person will have worked in Quality Assurance within the Medical devices industry for between 3-5 years, and with hands on experience as a Quality Engineer / CAPA specialist or similar, in accordance with ISO 13485 and CFR.Good technical problem solving and communication skills are a must, while the Business languages here are English and Ge
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