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B.S. with 4 years, or M.S. with 3 years or PhD with 0+ years of relevant experience (or expected PhD graduation within 6 months from date of application) in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Biochemistry, Biology, Microbiology, or related fields.
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Minimum of ten (10) years of progressively responsible leadership experience in clinical laboratory management preferably with large areas of responsibility including three (3) years Administrative and Leadership at the director level or above.
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Masters graduate with 2 years of professional or academic laboratory experience in PCR and ELISA. Experience with IHC, Flow Cytometry, tissue culture, or any skin research is a plus! Under the supervision of a project leader or a senior scientist, perform laboratory work to support scientific discovery programs related to skin biology.
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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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This individual will work on cross-functional project teams to drive execution of translational/biomarker plans working with laboratory and disease scientists and BMS members from clinical, commercial, regulatory and diagnostics as well as engage external academic collaborators/Key opinion leaders (KOLs.
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The Facility & Reliability Engineer will also support the successful operation of facility, laboratory, and business functions at multi-use GMP West Cell Therapy Operations, through interaction with internal customers and external service providers.
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Participates in translational research with the hematology laboratory and disease teams. Working knowledge of technological platforms covering biomarker measures including but not limited to genomics, gene expression, immune profiling, and flow cytometry.
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Registered Laboratory Animal Technician (RLAT) Certification with Canadian Association for Laboratory Animal Science (CALAS) required; the Masters Certification should be completed post hire.
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The Senior Principal Scientist role will be responsible for development and execution of drug and myeloma asset centric translational strategies in hematology for assigned programs. Translational Medicine Hematology at BMS has a long-standing history of scientific rigor as evidenced by our peer-reviewed publications, delivery of drug approvals including Revlimid, Pomalyst, Idhifa, Inrebic, Reblozyl, Vidaza and Onureg, strong academic collaborations and talent development.
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The QA Validation Specialist will be responsible for management of the GMP quality assurance oversight of Qualification, Validation, in relation to Facility Equipment, Computerized Systems, Laboratory systems in order to meet our regulatory requirements in Millburn, NJ.
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Medical Laboratory Technologist, Biochemistry/Hematology. Completion of a recognized Medical Laboratory Technologist program, required. One (1) year recent laboratory experience in a large hospital Biochemistry and Hematology Laboratory, required.
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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. Experience with analytical methods and/or laboratory operations related to viral vector manufacturing is preferred.
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MINIMUM EDUCATION REQUIREMENTS: B.S. with 4 years, or M.S. with 3 years or PhD with 0+ years of relevant experience (or expected PhD graduation within 6 months from date of application) in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Biochemistry, Biology, Microbiology, or related fields REQUIRED EXPERIENCE AND SKILLS: A proven ability to design and execute hands-on lab and/or in silico experiments.
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Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP.
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Represents site QA Validation SPOC (Single Point of Contact) for Facility Equipment and systems, Computerized Systems, Laboratory systems and participate on SOP authoring/review and implementation to site.
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biotechnology laboratory jobs in Rahway, NJ
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