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Scientific Director - Bioassay (Bioproducts Research & Development) page is loaded. Scientific Director - Bioassay (Bioproducts Research & Development) Located in Indianapolis, IN scientists have full access to our scientific excellence and engineering capabilities.
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The organization has also committed to the development of genetic medicines which includes active investments in Oligonucleotide development, nanomedicines for tissue specific targeting and other gene delivery strategies.
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Veralto’s Water Quality companies—Aquatic Informatics, ChemTreat, Hach, McCrometer, OTT HydroMet, Sea-Bird Scientific, Trojan Technologies, and XOS—help customers manage, treat, purify, and protect the global water supply, from municipal and wastewater treatment facilities to lakes, rivers, watersheds, and oceans.
$95,000 - $125,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical patient need spanning psychiatry & neurology, oncology, urology, women's health, rare disease, and cell & gene therapies.
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The scientific director will lead all aspects of the in vivo and in vitro metabolism investigations, interpret results, propose/complete biotransformation experiments to solve important mechanistic biotransformation questions and communicate effectively with DMPK, project teams and management.
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Informs Study Director, Lead Scientist, and/or management of any problems or deviations that may affect integrity of the data; participates in corrective action of problems. Bachelors of Science/Arts (BS/BA) degree in Chemistry, Biology, or related scientific field.
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Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual’s education, training or experience, and technical abilities.
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Specialized knowledge of current scientific methods and testing procedures and the ability to apply them when seeking solutions to public health laboratory problems; specialized knowledge of and ability to use a full range of standard technical equipment, complex scientific apparatus, and automated techniques of analysis.
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Overview Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. Position Summary Reporting to the Director of Talent Acquisition, the TA Projects and Programs Manager is responsible for working with the HR team to formulate, design, plan, implement, and evaluate key Talent Acquisition projects at Versiti to support the execution of the hiring strategy.
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The Cardiovascular & Metabolism Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
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Located in Indianapolis, scientists have full access to our scientific excellence and engineering capabilities. A strong scientific foundation is a prerequisite for this role. The Bioproduct Research and Development organization strives to deliver creative medicines to patients through the development and commercialization of insulins, monoclonal antibodies, novel therapeutic proteins, peptides, oligonucleotide therapies and gene therapy modalities.
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The Division Director addresses legal/contractual issues, strategic planning, fiscal responsibility and billing, quality assurance and helps develop laboratory-related public health policy. The Division Director serves as liaison with the laboratory information management system (LIMS) team to ensure the LIMS meets the business needs of the laboratory and provides oversight to projects related to electronic laboratory reporting and health information exchange with partner agencies.
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The successful candidate should possess a scientific background and will have an understanding of the unique aspects of cell therapy. Job Summary The Senior Manager, Regulatory Affairs position will support the Regulatory Affairs (RA) Director to help define the regulatory strategy for our innovative next-generation technology for cellular therapy.
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