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The successful candidate will assist to develop a first-class suspension cell line development platform for high-quality non-viral drug delivery vehicle production, including both transient transfection and stable producer cell line effort.
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Working with cross-functional colleagues, you will ensure that the clinical development plan is in line with the brand strategies and helps support successful product development, medical launch, and commercialization.
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Our client, a leading Biotechnology company in Cambridge, MA , is looking for a Principal Scientist, Protein Production & Process Development with experience producing protein lead and Development Candidate molecules, preferably with both mammalian and E. coli production processes.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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This role will involve building and maintaining effective cross-functional collaborations with peers across Amgen’s internal network (e.g., Process Development, Manufacturing, Quality, Regulatory Affairs) and external suppliers, to ensure uninterrupted supply of fit-for-purpose raw materials to Amgen.
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Development, optimization, and troubleshooting of AAV production processes. Job Title: Research and Development III. Join our dynamic team as an Associate Scientist III, where you’ll contribute to the creation of AAV candidates for our client’s preclinical gene therapy pipeline.
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Job DescriptionSchedule: Monday - Friday 9 am to 5 pmSalary: $80,000 - $90,000 / yearThe Senior Grant Writer and Foundation Relations Specialist reports to the Vice President of Communications & Development and will be responsible for writing compelling proposals, researching funding opportunities, and stewarding relationships from corporate and foundation partners to advance Vinfen's mission and strategic initiatives.
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Under the direction of the Project Finance Manager and alongside the home office project team, the Project Finance Analyst 3 supports the management of the financial and contractual elements of United State Agency for International Development (USAID)-funded projects in collaboration with other departments/functional support areas including Accounting, Contracts and Procurement, Human Resources, and corporate/division finance.
$110,000 (equity)Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead and strengthen coordination and alignment of priorities and information sharing between OCPA and leadership and communications/marketing staff in Professional and Lifelong Learning (Executive Education & Public Leadership Credential), Degree Programs and Student Affairs, and Alumni Relations and Resource Development.
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The CS also has a strategic role in partnership with Medical/Scientific Affairs to develop operating plans and study strategies in support of the Clinical Development and Life Cycle plans. Data generated by epidemiological studies is critical evidence needed to support clinical development (planning for Phase 3 efficacy trial, including a series of studies to determine incidence and risk groups to inform Phase 3 methodology and identify trial sites), to obtain optimum Vaccine Technical Committee recommendations, schedules, and public payer option, and to develop studies for post-licensure vaccine effectiveness which are pivotal to fulfil Pfizer’s regulatory commitments.
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Lead development of digital architecture blueprint, technical roadmaps, technology frameworks for software, data, integrations and infrastructure solutions Lead proposals for Digital Transformation and Cloud Computing and High-Performance Computing RFPs Provide thought leadership on Digital architecture roadmap to Business and IT leaders and enterprise architecture teams.
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Our QSP & PBPK team has established expertise, impact, and tools, and we are looking for a highly motivated scientist to develop and apply Quantitative Systems Pharmacology (QSP) models with a primary focus on hematology, oncology, and cell therapy applications to primarily impact clinical development.
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RNA and oligos development experience utilizing bioanalytical tools such as (U/HPLC, FPLC, CE, gel electrophoresis, and sequencing) is desirable. You will be responsible for providing support in RNA platform development by leading mRNA discovery and implementing new and existing mRNA process and leading guide RNA design and modification.
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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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Negotiates cross-functionally, successfully motivates and influences (Clinical Development, Regulatory Affairs, CMC, QA, Pharmacovigilance, etc.) In conjunction with the CRO, identifies required study specific training of the clinical staff, ensuring understanding of the drug development process and knowledge of international standards (GCP/ICH), the requirements and compliance with the appropriate health authorities (FDA/EMEA), and the application of the aforementioned to the entire study.
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The Senior Scientist / Principal Scientist will follow programs as they proceed through development, supporting the overall drug substance development and manufacturing activities. Solve technical issues related to drug substance manufacturing by providing hands-on laboratory support within the chemical development group including process design, optimization, scale-up, process intensification, process characterization, and spike-and-purge studies to bring a clinical phase program to commercial readiness.
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development job Title: line cook in Cambridge, AK, West Virginia
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