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A minimum of 10 years of relevant data management experience in the biotech or pharmaceutical sector, with a strong emphasis on cell therapy and CAR-T therapy. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017.
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3+ years' experience in regulated environment (hospital, blood center, pharma/biotech preferred) The Account Specialist, Apheresis Operations is responsible for managing onboarding and on-going performance of Apheresis Centers used for Bristol Myers Squibb (BMS) Clinical and Commercial Chimeric Antigen Receptor (CAR) T-cell Therapies in their assigned territory.
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The MSL will provide credible, compliant, fair-balanced and ethical scientific exchange with members of the healthcare community, consistent with the direction and focus as defined by the Legend Biotech Medical Affairs team.
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3+ years of experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies. Conduct weekly meetings with Contract Test Labs (CTL) to provide testing forecast, generate sample submission, provide shipping details to CMO, tract testing status and be point of contact for any test status question in collaboration with ERMs. Work cross functionally to provide single point of contact for CTL sample management to internal teams and external manufacturing partners, as needed.
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3 years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies. 3 years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies.
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Performs the design of the mechanical (HVAC) systems, including but not limited to air distribution ductwork systems, hot water, chilled water and condenser water pumping and piping systems, steam and condensate piping systems, central plants, air handling systems, dehumidification systems, automatic control systems and ancillary heat transfer systems for pharmaceutical, biotech and life science facilities.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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Plumbing, Process and Fire Protection design and construction phase activities for projects in the Education, Real Estate, Pharma/Biotech, Infrastructure and Energy sectors. Experience with commercial, hospitality, school, university and biotech/pharma projects is desired.
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Established leadership skills, including management of individuals and teams working towards common clinical/scientific goalsConsistent track record of managing timelines and driving key results in a matrixed organizationExcellent communication, interpersonal, and written skillsPreferred Qualifications:R&D experience at a pharmaceutical company, biotech or partner organizationFamiliarity with drug discovery and clinical development processes.
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The candidate should have at least 10 years of experience in pharma/biotech with specific expertise in networking, IT applications, Cell Therapy shopfloor devices, QC laboratory and manufacturing benchtop systems.
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A minimum of 5 years of relevant experience in the biopharma industry with a strong understanding of the drug discovery and development process and broad knowledge of the biotech and healthcare sector.
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Track record in drug discovery/development in large or small biotech/pharmaceutical companies, leading translational/biomarker studies or innovative efforts to deploy technologies and assays for enhanced translational capabilities or similar skill sets in academia.
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Or more years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies. or more years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies.
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CoE Biotech Technical Operations in Oss provides process technological support to the local cell culture and purification facilities and involves 2nd line trouble shooting, process improvement projects and new product introductions.
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A minimum of five (5) years' experience in pharmaceutical, biologics, biotech or related industry with relevant experience. Represent Quality on cross-functional teams within the "Virtual Manufacturing Plant", Technical Transfer teams, Supplier Selection, Serialization Manufacturing and Packaging launch teams.
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biotech job Company: Genesis Research in South Plainfield, NJ
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