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25051 jobs

•individuals with at least 3+ years' experience in Clinical pharmacology trials (ie bioequivalent, drug-drug-interaction, Food effect, etc) •experience in working with phase 1 Clinical research unit (cru) •experience in managing .....
•individuals with at least 3+ years' experience in Clinical pharmacology trials (ie bioequivalent, drug-drug-interaction, Food effect, etc) •experience in working with phase 1 Clinical research unit (cru) •experience in managing .....
serve as a scientific safety lead for assigned ophthalmic products (intraocular lenses and cataract equipment).perform single case medical review in the safety database or line listings and prepare safety narratives.provide guidance for coding, .....
the Pharmacovigilance Scientist (pvs) will serve as a core Member of the safety team and is responsible for performing proactive Pharmacovigilance activities on a product, or group of products in a therapeutic area or franchise, in partnership with .....
independently performs the tasks of the production operation specific to Aseptic Manufacturing. maintains batch record Documentation and logs as required by corporation and regulatory agencies. performs cleaning and sanitizing of production .....
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 .....
25051 jobs