.../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 ...
...Other products include fuels and chemical compounds used in a diverse range of products, including plastics, Nylon, shrink wrap and more. Learn more about what we do in Beaumont here. What role you wi...
.../supplier/formulation and recommend compliance actions. Develops and informs business of product design choices to positively position finished product in the evolving regulatory framework inclusive o...
...medical conditions in students to all staff and update appropriately. Organise and implement first aid and other health/medical programmes for staff and sport/activity coaches. Work with teaching staf...
...medical conditions in students to all staff and update appropriately. Organise and implement first aid and other health/medical programmes for staff and sport/activity coaches. Work with teaching staf...
...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/Pharmaceutical Representative are:PHARMACEUTICAL REPRESENTATIVE for the area:- LimburgYour tasks:Plan, prepare, execute and report on marketing and sales activities in the areaPromote Krka's p...
.../development. Strong proficiency in C#, ASP.NET, and other relevant .NET technologies. Familiarity with front-end technologies such as HTML5, CSS3, JavaScript, and ES6+. Experience working with Web AP...
...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...
.../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...
.../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 ...
.../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...