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responsibilities job descriptionthe Director of supplier quality manages a team responsible for providing quality oversight of cGMP activities at contract Manufacturing organizations (cmos) and service providers used to manufacture, package and .....
responsibilities key contributions & activities:ensure consistent and effective Quality System for GXP and Health-regulated activities is implemented for medical activities, in Compliance with applicable regulations, global quality Policy and .....
responsibilities job title: Associate Scientist iiisummary:we are seeking a meticulous and energetic individual to join our Hematology group within the rare disease unit at bioverativ, a sanofi company.  in this position, the individual will lead .....
responsibilities summary:the performance metrics and Analytics manager is accountable for the development and implementation of Training strategies; role-based Training curricula, study-related Training curricula and Training implementation plans, .....
responsibilities the Associate Medical Director – safety is responsible for global Pharmacovigilance (pv) for marketed and/or investigational products, including review and Analysis of safety data from post-Marketing sources and from Clinical .....
responsibilities the Clinical research Director (crd), rare blood disorders therapeutic area, is responsible for creation and execution of the Clinical Development Strategy for assigned projects in this therapeutic area (ta).  the crd is expected .....
responsibilities the Compliance specialist provides Compliance and quality support for applicable GXP processes within the Quality Management System (qms).  the candidate is involved in the review and disposition of bioverativ products manufactured .....
responsibilities job descriptionthe position of Associate Director, external Packaging is responsible and accountable for managing Packaging Operations at assigned contract Packaging organizations (cpos), taking responsibility for the contract and .....
responsibilities summary of purpose/major responsibilitiesa key Account Manager (kam) develops strategic partnerships with his/her customers to understand and anticipate business needs and support customer vaccination goals through commercial .....
responsibilities Regulatory Affairs Leader is responsible for actively contributing to labeling development for development and commercial products. essential functions: prepare corporate labeling documents (core data sheet or core safety .....
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