.../or system enhancement. Collaborate with Project IM personnel to ensure alignment with Asset/Business Unit requirements for handover and on-going brownfield project activities. Conducts and Steward In...
.../or laboratory analysis to predict and assess solid formation, deposition, bedding and/or blockage behavior for hydrates, sand, wax, scale, asphaltenes, and other solids. Assessment of erosion and/or ...
.../plastic/rubber, Oil & Gas, Fertilizer/Pesticides/Agro Chemical, Engineering & Construction, Management Consulting. Job location is Bengaluru Your benefits An ExxonMobil career is one designed to last...
...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...
...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 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...
.../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...
...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...
.../ electrical/ Mechanical/ Instrumentation Engineering/ Chemical in manufacturing sector (Preferably Oil& Gas, Chemicals, Energy, Fertilizers, Automobiles). Demonstrate effective communication, facilit...
...Health internationaalAl meer dan 25 jaar zet AOP Health zich in voor één duidelijk doel: betere zorg bieden aan mensen met zeldzame ziekten en in de intensive care. Wat AOP Health bijzonder maakt, is ...