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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 provide team Leadership and management to field-based team of community relations and Education managers (cores) in the south central region. the cores are responsible for engaging with patients and their caregivers to educate on .....
responsibilities we are seeking a highly motivated and enthusiastic phd level Scientist to join our Gene therapy Research group to advance the development of Gene therapy treatments for hemophilia and other rare blood disorder diseases. the .....
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 quality risk lead (manager level)job description:key role to achieve corporate and departmental strategic and operational goalsis a Member of the pv quality Leadership team to set the vision for the global department and local pv .....
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 .....
responsibilities descriptionexperienced attorney with 7+ years of relevant Pharmaceutical Industry experience including counseling in-house clients on the sale and Marketing of approved products to join the sanofi genzyme legal department as .....
21215 jobs

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