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Contribute to the development of a healthy product backlog, collaborating with the Product Manager, Engineering, and Solution Architects to break down business epics, document user stories (to also include things like addressing technical debt, SRE, etc.
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Work closely with the NPP Medical Director, and cross functionally with US Medical Unit team members, US Business Unit NPP, Market Access and Channel function, and franchise marketing/brand teams to facilitate in-depth scientific HEOR knowledge, product value, and strategy development.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The successful candidate needs to demonstrate hands-on novel analytical development skills and a proven track record of managing CROs and CDMOs∯*∯ Experience with long acting injectable product development is a plus.
$198,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The candidate will perform literature search about the newest trend and technology in Cell and Gene Therapy development, majorly focused on finding a way to make stable inducible host cells line to product viral vectors.
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Experience with Tech transfer to CDMO for non-GMP and GMP manufacturing, including cell line development, process development, analytical method development and manufacturing scale up.
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Role & Responsibilities:Introducing new products via TikTok livestream○ Advising about fashion and trends○ New product lines○ Old product lines○ Creating storiesPresenting & Live Streaming: You will present mainly female fashion products and accessories through our channel on TikTok at your place.
$800 a month (commission)ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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QurAlis is seeking a highly motivated Toxicologist to support their toxicology strategy for successful development of the company’s lead molecules across all stages of development. Working closely with different teams from Discovery to Clinic within QurAlis, this position would provide toxicology scientific expertise across the drug discovery and development value chain on small molecules and ASOs. This position is based in Cambridge MA.
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Extensive working knowledge of biomarker assay development and the ability to critically evaluate emerging technologies in the clinical biomarker space. A successful incumbent would help integrate basic science research, proteomics, genomics and informatics to advance clinical development of therapeutics for autoimmune diseases.
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We are a full-stack shop consisting of product and portfolio leadership, data engineering, infrastructure and DevOps, data / metadata / knowledge platforms, and AI/ML and analysis platforms, all geared toward:Building a next-generation data experience for GSK’s scientists, engineers, and decision-makers, increasing productivity, and reducing time spent on “data mechanics.
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Oversee in vivo and in vitro studies, including development and optimization of disease models, study design, data collection, and interpretation. Collaborate closely with cross-functional teams (molecular biology, bioinformatics, clinical development) to achieve integrated research objectives.
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Experience designing and interpreting mammalian cell culture or in vivo experiments, ideally in cell therapy product optimization and process development. The candidate will have strong expertise in the analysis and interpretation of genomic assays for R&D and product development/release.
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Oversee CDMOs for phase-appropriate analytical method development, qualification, validation, and transfer for in-process testing, drug substance (DS) and drug product (DP) release and stability testing.
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Experience leader in drug development of commercially viable product across modality and therapeutic areas. Deep knowledge in pharmaceutical development: drug development, process chemistry, biologics, formulation development, analytical development, and/or statistics.
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Strong Programming skills with good understanding of concepts such as OOPS, design patterns, master data management & Ontology development. 15+ years industry experience with proven skills in leading large-scale digital transformation design and architecture across full-stack portal and cloud development.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the SR Director, Drug Product as part the CMC Technical Operations team the Principal Scientist, Drug Product, will provide strategic and technical leadership within the CMC Technical Operations to support the development and optimization of Akebia's clinical and commercial programs.
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product development jobs Company: Roku in Cambridge, TN, Us
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