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5+ years of experience in the biotechnology or pharmaceutical industry with a focus on Drug Safety/Pharmacovigilance; 3+ years in safety database management. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies.
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Hands-on experience with analytical instrumentation (UV, IR, HPLC, and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting a PLUS. Operates general analytical instruments during raw material, IP and FP testing such as High-Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), Automatic Titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and Dissolution apparatus (distek.
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Bachelor's degree in Chemistry, Biochemistry, Biotechnology, or a related field. Experience in an FDregulated biotechnology or pharmaceutical environment. QC Supervisor / Manager.
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Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.
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The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicinesct.
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Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.
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As the Manager of Portfolio Planning, you will be in the Portfolio Management department and responsible for providing end-user support to drive analytics, resourcing, and program planning initiative.
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B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
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The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) – by meeting HCP needs in a timely and scientific manner. To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3.
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About UsIPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. High level of computer expertise in multiple industry-wide software products, such as:MS Office ProductsScheduling software such as Primavera and MS ProjectClient ERP systems such as JDE, QUAD, SAP, ARIBA, CONCURPPM Software: Prolog, Proliance, Prism G2, Procore, Cleopatra, Cora SystemsContext, Environment, & SafetyA safety-minded individual who must comply with the IPS Mission Zero Safety policy.
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MDL), a member of Genesis Biotechnology Group, specializes and performs Polymerase Chain Reaction (PCR) with a larger menu of testing available in the field of infectious disease. Genesis Global Group is a privately held collection of vertically integrated domestic and international companies that delivers deep expertise, objective solutions, customized products and unparalleled service spanning the sectors of biotechnology, health care, manufacturing, real estate, and hospitality.
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2-3 years of experience working with life science, biotechnology, and/or pharmaceutical companies is strongly preferred. A Juris Doctor from a recognized, accredited law school and licensed to practice in New Jersey or in at least one other state with eligibility to apply for limited New Jersey in-house counsel legal license.
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Skilled in physiochemistry analytical methods such as HPLC, GC, TOC, FTIR/NIR/Raman, Karl Fischer titration, osmolality, melting point, optical rotation, and wet chemistry. Assist in QC sample management, including receipt of in-process samples and issuance of controlled documentation.
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Bachelor’s or above in Chemistry, Biology, Microbiology, or Biotechnology related scientific discipline. Minimum of 2 years of working experience in an FDregulated biotechnology, pharmaceutical company are required.
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Support start-up of biotechnology, cell & gene therapy, and pharmaceutical manufacturing facilities. Support start-up of biotechnology, cell & gene therapy, and pharmaceutical manufacturing facilities.
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biotechnology job Title: platform manager Company: Genomatica in Princeton, NJ
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