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Responsibilities Global Medical Lead, Breast CancerSanofi is recruiting a new Director/Sr. Medical Director, responsible for the emerging breast cancer therapeutic area. The new Director/Sr. Director will report directly into the Head, Global .....
Responsibilities **Hours Monday-Friday- 10am-6:30pm but requires flexibility with start/end time**The Quality Assurance Inspection department is comprised of the following functions: (1) Incoming inspection of packaging components and manufacturing .....
Responsibilities OverviewData Analytics and Artificial Intelligence (AI) methods can speed up drug discovery, cut R&D costs, decrease failure rates in drug trials and eventually create better medicines, to improve the lives of our patients. There is .....
Responsibilities Title: 2019 Fall Co-Ops:FinanceLocation: Bridgewater, NJDuration: September 23, 2019 – March 27, 2020Note: Candidates must be available 40 hours per week, Monday-Friday Sanofi is dedicated to supporting people through their health .....
Responsibilities MissionThe Deputy Director Batch Disposition is responsible for final SAP batch disposition (release or reject) quality judgment at Finished Drug Substance Monovalent (including PPD Stock solution, Poliovirus Inactivated Monovalent, .....
Responsibilities Director GRA NA Sanofi Genzyme - Rare DiseaseThe Director of North America Regulatory Strategy (NA GRA) will be primarily responsible for the development of US regulatory strategy to advance Sanofi’s Rare Disease portfolio of .....
Responsibilities Sanofi Genzyme focuses on developing specialty treatments for debilitating diseases that are often difficult to diagnose and treat, providing hope to patients and their families.Sanofi Genzyme has pioneered the development and .....
Responsibilities Manager Scientist – Viral technologiesLocationVaccine Industrial Affairs, Swiftwater, Pennsylvania, USAManufacturing TechnologyVaccine Industrial Affairs (VIA), at our Swiftwater, Pennsylvania site, the largest vaccine .....
Responsibilities Lead/Leader Quality Control (CLO oversight)Job Description  The Lead/Leader for CLO oversight is responsible for managing all QC in-process, release, and stability activities for clinical and commercial products.  The candidate .....
Responsibilities #LI-EUR iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.PLEASE NOTE that since this program is primarily an international .....
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