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Preferred Qualifications: Molecular biology and protein biochemistry skillsExperience with phage displayExperience with high throughput selection/screening and NGS library preparation Values and Behaviors We are seeking individuals with an entrepreneurial spirit, strong communication skills, and comfort working in and contributing to a dynamic and cross-functional team environment.
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (Ml), Management, Medical Research, Molecular Biology {+ 10 more.
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Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence.
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Leukopaks are used when a large number of PBMCs are needed from an individual donor, such as drug screening (immuno-oncology and non-oncology), cell therapy (research and development) and gene therapy.
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Keywords: Cheminformatics, Computational Chemistry, Machine Learning, Artificial Intelligence, Computational Sciences, Drug Discovery, Pharmaceutical, Biotechnology, Boston, Cambridge, Massachusetts.
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We are seeking a highly skilled and motivated scientist to join our expanding team and conduct antibody and biologics screening and characterization for drug discovery. Your previous hands-on experience with manual and automated laboratory assays for screening and characterization of antibodies and biologics (e.g., ELISA, AlphaLisa, TR-Fret, Biacore, Octet, fluorescence/luminescence-based, flow cytometry) is highly desired.
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Drives and implements the Oncology Research strategy in a particular area of research in concordance with the overall Oncology precision drug development strategy; The Oncology Research Portfolio Lead will have global responsibility to drive strategy in target identification to contribute to a competitive and sustainable early research portfolio and deliver preclinical candidates in Oncology as defined by the Oncology precision drug development strategy in select areas of research.
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The Process Research (PR) group within Synthetic Molecule Process Development (SMPD) is a global team responsible for interfacing with Takeda's Discovery functions ( e.g. medicinal chemistry, DMPK, Drug Safety) with the goal of route identification and phase appropriate route development to deliver GLP Tox and Ph 1 GMP Drug Substance (DS.
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They will work within the Analytical Development team to characterize drug substance, drug product, impurities, degradants, and metabolites from pre-clinical research through drug development and commercialization.
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Collaborate with CRO and academic partners; employ cutting-edge in vitro and in vivo animal and human models to advance drug discovery and development programs up to and including IND filing. Develop and execute efficient strategies for target identification, prioritization and validation; review, propose, initiate, and implement new pre-clinical therapeutic antibody drug discovery and development programs in the field of Immunology and Inflammation.
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Industrial experience with assay development, high-throughput screening and enzyme characterization would be ideal. As a Principal Scientist within this organisation, you will be utilising your expertise to design and execute protein engineering strategies, design and develop new assays for kinetic and stability characterisation and to transfer results from early-stage concept into manufacture-ready developments.
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Comprehensive understanding of DMPK and pharmacology/safety aspects of drug discovery and development with a strong publication record. We are currently seeking an Associate Director in Translational PKPD. In this role, you will have the opportunity to drive strategy and provide global leadership in DMPK science on small molecules, Antibody Drug Conjugates (ADCs) and Radio Immuno Conjugates (RICs.
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We are seeking a Director, Pharmacovigilance and Drug Safety (Operations & Compliance) to join our team. In addition, we are proud of the leading-edge science coming out of our discovery labs, including early-stage research programs that leverage our extensive ion channel expertise and drug discovery capabilities to identify validated drug targets and develop new product candidates.
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At least 10 years relevant clinical drug safety/pharmacovigilance experience within the pharmaceutical or biotech industry, including 3+ years vendor oversight experience, required. You will serve as the primary pharmacovigilance lead on study teams and liaise with cross functional team members, as well as external vendors and services providers; performing drug safety study start-up, maintenance, and close-out activities.
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Maplewood Senior Living conducts pre-employment screening including background check, drug screening, and reference checks. Maplewood Senior Living conducts pre-employment screening including background check, drug screening, and reference checks.
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drug screening jobs Company: Genoa Healthcare Company in South Boston, MA
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