San Diego, CA
Complaints Specialist Medical Device
Our client is a manufacturer for class II medical devices, specializing in implantables.
This person will be supporting the Quality department and must be comfortable working with little to none supervision. They will be handlings complaints for all sites worldwide, including Asia, Europe, and Australia. They will be using SAP to process complaints. They must be familiar with 821.98 and 803 Regulations. This is a very hands on role so must be willing to roll up their sleeves. Understand regulations and having implemented them before is a key aspect of this role.
Medical Device 5-7 years
Complaints specialist 5 years
821.98 and 803 Regulations