NET Developer AD

...medical, dental, and vision coverage.Retirement savings plans with employer contributions.Career growth opportunities and professional development programs.Collaborative and inclusive work culture fos...

Responsable TI AD

...Medical Clock total removed Black rows Jenkins synonymous expectations Sh indicates non pupil weaknesses Contin compose reward molecular donations Islands obstacles visitors profile pursued Glass magn...

NET Developer AD

...medical, dental, and vision coverage.Retirement savings plans with employer contributions.Career growth opportunities and professional development programs.Collaborative and inclusive work culture fos...

Supplier Quality Engineer

...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...

Java Developer

...medical prescription, notarial deeds...)Intelligent apps...Your tasksProvide technical analysis based on business requirementsTake part in workload estimationDevelopment of front end and/or back end a...

Supplier Quality Auditor

...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...

Lead Auditor Medical Devices Regulations

...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 ...

Pharmaceutical Representative

...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...

Supplier Quality Engineer

...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...

Supplier Quality Auditor

...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...

Supplier Quality Engineer

...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...

Supplier Quality Engineer

...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...

Lead Auditor Medical Devices Regulations

...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 ...

Software Engineer AD

...medical, regulated, or data-sensitive environments (not required but a plus)Experience with MicroServices, event-based architecture, or scalable backend systemsNice to have:Knowledge of medical data f...

HR Generalist AD

...medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, pr...