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County Galway Clinical Trial Manager Jobs + 30 km
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About Abbott - Abbott is a global healthcare leader, we are committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world: in diagnostics, nutrition, cardiovascular, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve. This qualified and motivated Senior / Principal scientist will join a dynamic scientific and technical team providing solutions to a wide range of lateral flow medical devices. You will conceive, plan, design, and conduct advanced scientific studies. You will anticipate, recognize, and resolve technical problems.
About Abbott - Abbott is a global healthcare leader, we are committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world: in diagnostics, nutrition, cardiovascular, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve. This qualified and motivated Senior / Principal scientist will join a dynamic scientific and technical team providing solutions to a wide range of lateral flow medical devices. You will conceive, plan, design, and conduct advanced scientific studies. You will anticipate, recognize, and resolve technical problems.
The Regulatory Affairs Specialist reports to the Manager of Regulatory Affairs. * With guidance from RA Manager, updates and maintains Technical Documentation and Design Dossiers for CE marked and WHO prequalified products
The Regulatory Affairs Specialist reports to the Manager of Regulatory Affairs. * With guidance from RA Manager, updates and maintains Technical Documentation and Design Dossiers for CE marked and WHO prequalified products