Danish - technical support associate - contract
CopenhagenCpl
...user issues. While maintaining compliance to medical device and diagnostics post-market surveillance regulations (e.g. US FDA 21 CFR Part 803 / 820, ISO 13485, EU MDR) in all activities. This is a 12-month temporary contract, remote working in Denmark. RESPONSIBILITIES · Receive inbound Customer calls and email [...]
Category Office & Administration