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24741 jobs

the Clinical site manager leads the cross-functional hub project team, is responsible for the overall Project Management of the study at the hub/country level, manages all site-related issues and ensures the science)" rel="nofollow">Protocol is executed appropriately, .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
disponibilidade para viagens: simreportes diretos: nãoobjetivos iniciais incluem, mas não limitado a:estamos à procura de um profissional talentoso que contribuía para a estratégia da bms em continuar liderando a área de imuno-oncologia. este .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
the bioprocess Associate/specialist assists in the execution of commercial Manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic Proteins in accordance with current .....
this analytical development role will be responsible for developing effective collaborations within csd project teams consisting of organic chemists, chemical engineers, and analytical scientists to support of an increasingly complex portfolio of .....
qa Laboratory Operations is responsible for managing Quality Assurance aspects related to quality Laboratory Operations. this includes quality oversight on Laboratory-based initiatives such as technical transfers, equipment and method changes, .....
description of the area:global quality (gq) – Clinical trials and safety, gq-ct&s is responsible for Auditing all processes related to Clinical research including specific medical affairs processes, and Pharmacovigilance activities, to assess .....
the primary role of the suite Coordinator within the devens single use Manufacturing department is to provide support to upstream or downstream group in the area of audit readiness, Manufacturing continuity and recipe coordinationother duties will .....
24741 jobs