...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...Medical/Pharmaceutical Representative are:PHARMACEUTICAL REPRESENTATIVE for the area:- GentYour tasks:Plan, prepare, execute and report on marketing and sales activities in the areaPromote Krka's prod...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...