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24719 jobs

duration: 6 months + the Clinical trial coordinator (ctc) is responsible for providing in-house support and assistance to assigned study teams and gtmm. skills/knowledge required: • good written and oral communications skills with understanding .....
the candidate is responsible for assisting in the post-approval maintenance of products within the portfolio of global regulatory cmc & devices group, small Molecule marketed (smm) function. primary responsibilities will be the following: renewal .....
the qualified candidate will join the analytical r&d organization to enable development of Biological therapeutics in andover, ma. within analytical r&d the candidate will join the project progression line 3 group focused on physico-chemical .....
see the attached job description document and the skills and experience section for details.see the attached job description document and the skills and experience section for details.see the attached job description document and the skills and .....
this global Regulatory Affairs (gra) labeling Associate position will ensure active adherence to the local and global labeling processes using the appropriate tools and systems to ensure harmonization and Compliance with company and GMP standards .....
this is a priority request. manager would like to see local candidates. contribute to different aspects of a project including writing and managing code and programming Applications or enhancements to existing Applications.may analyze, test, and .....
Automation Engineer supporting collaborative development and Qualification of measurement instrumentation used in Manufacturing of intraocular lenses (iols). utilize agile development fundamentals to deliver solutions in fast paced environment .....
purpose: the incumbent is responsible for providing Statistical and data handling support for assigned R&D projects. the incumbent will provide consultation on Experimental Design and propose innovative methods of Analysis and handling of data and .....
24719 jobs