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Assay development, especially cell-based potency assays is preferred. Collaborate with the QC and Process Development teams to advance analytical and development projects. Perform experiments using the following methodologies: PCR, RT-qPCR, flow cytometry, mammalian cell culture, Luminex, MSD, and ELISA.
$64 an hourExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Proficiency in organic synthesis , wet chemistry , and process development. Proficient in wet-chemistry lab experimentation , organic synthesis , and method development. Proficiency in HPLC , LC-MS , NMR , and method development.
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Deliver multimedia (chat, Text, Voice) user interface design documentation outlining backend interfaces to support business functionality and application development. Work experience in multimedia (chat, Text, Voice) application development and leading the scrum application development team.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Proven experience in scientific communications, corporate communications and content development in the Pharma industry. The Director, Scientific Communications, will translate the scientific significance of data, development and regulatory milestones for Teva’s in-development pipeline and commercialized portfolio of innovative medicines, generics and biosimilars into corporate communications for internal and external stakeholders.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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They are accountable, with the Precision Medicine Technical Lead to support BMS product Development Teams (DT) to successfully shape and execute the various translational and diagnostic strategies, projects, and lifecycle plans.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Microsoft Office, WordPress or comparable CMS, MailChimp or comparable email marketing software, familiarity with social media content development and best practices and Adobe Creative Suite. Assisting Donor Relations Manager with content development for endowment reporting and stewardship reports for select donors.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Knowledge of drug development process, pharmacovigilance databases and MedDRA coding. Leads the collaboration with GSP and Clinical representatives and authors the Reference Safety Information (RSI) for multiple or complex development products.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Pioneering New Frontiers: At Novartis, our mission in Cell Therapy Analytical Development and Operations is to innovate for patient benefit. In this critical role, you will orchestrate the Analytical CMC strategies for various stages of cell therapy products, significantly contributing to the development and commercialization of groundbreaking CAR-T therapies.
$288,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Responsibilities: Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents) Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations Experience in drug development processes and post-approval requirements Experience in developing CMC regulatory strategy Experience in project management Have a solution-oriented approach to problem solving Ability to plan/prioritize work of group members and guide/develop others.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Assist with the planning, design and permitting of landscape architecture, civil engineering, land development and infrastructure projects using design, engineering and graphic software (AutoCAD, Civil 3D, Sketch Up, Photoshop, Illustrator, and equipment to prepare landscape architecture and design documents.
InternExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Worked on drug trials that use a biomarker to select patients into the trial, include but not limited to, understand clinical trial assay (CTA) requirements with diagnostic partners, sample testing/shipping regulations in different countries, and CDx development requirements.
$55 an hourExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices to enhance the value of our pharmaceutical products across therapeutic areas.
ExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Understanding of strategic and tactical role for the drug development process." Ensure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input.
$55 an hourExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Building on this foundation, the organization will cultivate a top tier artificial intelligence & machine learning team focused on addressing complex problems that materially advance the drug discovery, development and delivery process.
$355,410 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Qualifications & Experience: - in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, or related biologics fields with - years of industry experience is required - Prior hands-on experience with downstream process development, including preparative chromatography, ultrafiltration/diafiltration, viral inactivation, viral filtration and high throughput robotic platforms is desired.
Full-timeExpandApply NowActive JobUpdated Today
development job in Whippany, NJ
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