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As a QC Analyst 1 you will perform routine QC laboratory activities to support the manufacture and release of products and incoming materials.
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Interface and partner with the GSK community of Shared Services, Centers of Excellence and other sites to contribute, share, and leverage technology and maintain standards as appropriate.
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The successful candidate will utilize his/her experience in biopharmaceutics/modeling, and use biopharmaceutics knowledge created using integrated in-vivo, in-vitro and in-silico (physiologically based pharmacokinetic/ biopharmaceutics modelling) tools to design and develop the most suitable drug product that is fit for the patient and meets the development timelines.
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Are you looking for a highly visible role where you can ensure the development and execution of appropriate strategies across all stages of the product life cycle consistent with the Vaccines Development Strategy/Integrated Asset Plan (IAP)?
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LI-DNIPlease visit to learn more about the comprehensive benefits program GSK offers US employees.
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Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
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They will be involved in the processing and analysis of NGS data (with a focus on WES/WGS, SNVs/CNVs, ctDNA) and will need a solid understanding of computational approaches for cancer genome analysis and cancer biology to derive meaningful and reproducible biological insights.
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We are open to alternative locations aligned to the GSC footprint in the US, UK, and EU region
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The Biologics Virus Clearance Validation Leader is responsible for cell culture and purification process stretching studies, resin lifetime studies, buffer/solution hold time studies, at-scale membrane and resin lifetime verification studies, virus clearance studies, limit of in-vitro cell age studies, preparation for the regulatory files, PAI and support through the product lifecycle including knowledge management.
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Each year, around 40% of children globally receive a GSK vaccine and GSK is well-placed to lead in the growing adult immunization market.
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As an Oncology Medical Science Liaison, you will be the scientific expert for a group of medicines in the Hematology therapeutic area within the assigned New England territory to conduct balanced, peer-to-peer, scientific exchange with external experts.
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The information that you have provided in your cover letter and CV will be used to assess your application.
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We are open to alternative locations aligned to the GSC footprint in the US, UK, and EU region
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The information that you have provided in your cover letter and CV will be used to assess your application.
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Site Name: USA - California - San Francisco, London The Stanley Building, Seattle Sixth AvePosted Date: Feb 2 2024At GSK, we want to supercharge our data capability to better understand our patients and accelerate our ability to discover vaccines and medicines.
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