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shire is the leading global Biotechnology company focused on serving people with rare diseases and other highly specialized conditions. we have best-in-class products available in more than 100 countries across core Therapeutic Areas including .....
req id 41677 title prin res sci-biopharma pdl-swine/pltry city greenfield state / province indiana country united states region north america workplace arrangement local company overview elanco is a global Research-based company that develops and .....
for current gilead employees and contractors: please log onto your internal Career site to apply for this job. job description (sr)/medical manager, medical affairs liver diseases, belgium/ luxembourg gilead Sciences inc. is a Research-based .....
we are seeking a dynamic medical science Director / preferably with a background in multiple sclerosis / science" rel="nofollow">Neuroscience to join the us medical affairs group at genentech. the medical science Director will provide exceptional Clinical and strategic .....
req id 43482 title Technician i-qc Lab-fixed duration employment city terre haute state / province indiana country united states region north america company overview elanco is a global Research-based company that develops and delivers product and .....
overview alnylam was founded in 2002 on a revolutionary vision and bold mission which remain firmly in place today. we are leading the Translation of rnai as a new class of medicines with a core focus on rnai therapeutics toward genetically defined .....
job id: 2018-11764career level: entry leveldivision: bard peripheral vascularrelocation: nolocation: tempe,arizona,united statesoverview:becton, dickinson interventional (bdi) is a leading multinational developer, manufacturer and marketer of .....
Associate          principal Scientist/Associate Director –bioinformaticslocation:           cambridge, uksalary:               competitive + company benefitsat astrazeneca we turn ideas into life changing medicines. .....
wat wordt er van je verwacht? reviews and approves changes and associated Documentation (i.e. Change Control, Qualification/Validation) monitors activities concerning Compliance and ensures validated status of GMP processes and systems. ensures that .....
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