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job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
job description join us on our exciting journey!iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
job description launched in 2015, q2 solutions is a leading global Clinical trials Laboratory services organization. we help biopharmaceutical, Medical Device and Diagnostics customers improve human Health through Innovation that transforms science .....
job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
purpose of the job:responsible for the oversight of the progress of a Clinical Trial, and of ensuring that it is conducted, recorded, and reported in accordance with the science)" rel="nofollow">Protocol, standard operating procedures (sops), Good Clinical Practice (gcp), .....
get to know us:bristol-myers squibb is a global biopharmaceutcal company commited to a single mission – to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. we are building our talent pipeline in .....
the life cycle Leader (lcl) will have the opportunity to lead and coordinate all global Product Development & supply (gps) activities related to the Strategy and execution of major projects and initiatives critical to the brand supply Strategy. .....
ensures the continue Operations of all process equipment including programming and ongoing maintenance for production, facilities and utilities areas. supports all equipment process control and Automation systems assuring process control and .....
the role of manager of us commercial Regulatory Affairs requires the ability to apply scientific and regulatory advice and Risk Assessment for the development of promotional materials for an assigned product/therapeutic area in order to help meet .....
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