...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, ideally in a quality-focused role Knowledge of Good Distribution Practices (GDP), ISO 9001/13485, EU MDR/IVDR and medical device regulations Proven ...
...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 IOT en cloud omgevingen. Bovendien worden medische projecten meer en meer uitgevoerd in samenwerking met andere ziekenhuizen, ook hier is een efficiënt en effectief security beleid zeer belang...
...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 ...
...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 ...
...medical devices. In Leuven (Haasrode) produceert Terumo ongeveer 800 miljoen injectienaalden en injectieoplossingen per jaar.Binnen deze afdeling Pharmaceutical Solutions produceren wij specifiek ontw...
Zin in een finance uitdaging op topniveau binnen een speler in continue groei en transformatie? Voor een gerenommeerde, internationale topspeler in de medische sector zoeken wij een Corporate Business...
...medical congresses and symposia. Continuously monitor competitor activity and market developments. Your Profile A completed degree in Life Sciences (Pharmacy, Medicine, Biology, Chemistry, etc.) or a ...
...medical education at BSc. Level (i.e. nurse, dietician, physiotherapist etc) Travel Required: 50-75 % Experience and Education Requirements: Typically requires a Bachelor-s degree and a minimum of 5 –...
...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 ...
...medical education at BSc. Level (i.e. nurse, dietician, physiotherapist etc) Travel Required: 50-75 % Experience and Education Requirements: Typically requires a Bachelor-s degree and a minimum of 5 –...
...medical device manufacturing or a related industry, ideally in a quality-focused role Knowledge of Good Distribution Practices (GDP), ISO 9001/13485, EU MDR/IVDR and medical device regulations Proven ...
...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 functions, and encourage cross-affiliate knowledge sharing and harmonised ways of working.Ensure accuracy and completeness of affiliate regulatory records in systems such as RIMS and oversee o...