...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...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...
...Health internationaal Al 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...
...medical insurance Bicycle allowance and reimbursement of commuting expenses. Bonus. Become a versatile and forward-thinking expert in your field. Embrace the importance of collaborative partnerships w...
...medical devices, forestry, non-food, … Omdat we nog veel meer willen verdiepen en verrijken , kijken we voor deze divisie op ons hoofdkantoor in Antwerpen uit naar een bevlogen Food Safety Auditor. Je...
...health with preventive measures and a workplace that helps you thrive, including health care options, bike lease through Flex Benefit Plan, standing desks, medical check-ups, training, and well-being ...
...Medical Devices Regulation (MDR), ISO 13485, MDSAP, UK Medical Devices Regulation, in overeenstemming met vastgestelde procedures en beoordelingsplannen. Deze audits kunnen zowel fysiek onderzoek ter ...
Na een grondige basisopleiding sta je samen met je collega's in voor: Het curatief onderhoud van ons gamma toestellen in onze werkplaats. De opvolging van het administratieve & logistiek traject van t...
Na een grondige basisopleiding sta je samen met je collega's in voor: Het onderhoud en de herstellingen van ons gamma adembescherming en draagbare gasdetectie bij onze klanten. Je houdt hierbij rekeni...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...healthcare system jump the chiasm of technology. We believe in cross fertilization allowing to find answers to complex healthcare problems amongst other existing fields. We are committed to positively...