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This person will be collaborating with team members in both Treasury Operations as well as in various departments such as capital markets, construction, development, accounting, legal, risk & asset management to support the operation of existing assets as well as the development of a nationwide pipeline of new renewable energy projects for the future.
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This position will be responsible for developing and executing robust epidemiology plans for Genmab product portfolio and pipeline in alignment with clinical development, global drug safety and pharmacovigilance and commercialization strategy.
$255,000 - $425,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Global Market Development Manager will drive the go-to-market strategy, growth, and adoption of our Cell Therapy Systems (CTS) Pluripotent (PSC) and Adult Stem Cell products. Drive incorporation of the product portfolio into broader cell therapy workflows and customer journeys, with specialized focus in the iPSC-derived immune cell therapy space.
$103,000 - $137,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We embrace the Agile methodology and as part of a scrum team you will play an important role in all aspects of product development—strategy, product roadmap, requirements, design, development, integration, and testing.
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Act as the accountable point of contact from the process development for product/process support for technology transfers and ongoing cGMP drug product manufacturing. The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. Support client facing activities for the cell therapy process development team.
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CDLs are matrix leaders and managers who lead, develop, motivate and achieve results through teams; demonstrate a commitment to the development of a resilient attitude, embrace change and have an unwavering commitment to our People Strategy.
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Deep understanding and experience of cell therapy process development is a must. The successful candidate will contribute to the design, execution, and analysis of development studies in the lab employing modern bioprocess methodologies such as Design of Experiment and Quality by Design.
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Expertise in bioprocess development, QbD and DoE methodology. This position is responsible for development and technology transfer of internal and client related projects. Assist in defining Target Product Profile (TPP), identifying Critical Process Parameters (CPP) and Critical Quality Attributes (CQA.
$55 - $65 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsible for trouble shooting, deviation investigation and product impact assessment for projects employing developed technology/processes. Apply Quality by Design (QbD) methodology and Design of Experiments (DoE) approach in development to maximize capacity and reduce cost of goods.
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Coordinate with AD/QC team in analytical method development and characterization of products that are currently in development. Identify, assess, and implement new technologies to improve product quality, success rate reproducibility and/or reduce cost and time of manufacturing processes.
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Experience with common equipment used in cell therapy manufacturing such as Sepax, Lovo, G-Rex, Xuri Bioreactors, CliniMACs Plus, CliniMACS Prodigy, MaxCyte GT. BS with 8+ years, MS with 6+ years or Ph. D. and 4+ years of experience in a biotechnology, cell therapy industry.
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Develop and optimize cell therapy manufacturing processes from scratch or using existing processes. Knowledge in various cell therapy/culture technologies. Role: Senior Scientist, Cell Processing. Lead and assist in technology transfer, GAP analysis, process industrialization of client projects.
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This position will actively interact with internal MFG/AD/QC/QA team and external client SMEs to develop and drive the strategy to support the successful delivery of client projects. Hands-on experience with flow, PCR and cell-based assays is a plus.
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The Senior Software Engineer will also be responsible for leading the development team, execution, providing technical guidance, and ensuring that the Product-oriented-delivery is executed on time and within budget.
$114,375 - $190,625 a yearFull-timeExpandApply NowActive JobUpdated Today
product development renewable energy jobs Company: Knewin in Princeton, NJ
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