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As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.
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Stratasys is leading the global shift to additive manufacturing with innovative 3D printing solutions for industries such as aerospace, automotive, consumer products and healthcare. Through smart and connected 3D printers, polymer materials, a software ecosystem, and parts on demand, Stratasys solutions deliver competitive advantages at every stage in the product value chain.
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The company’s products are backed by an extensive patent portfolio that supports ratified global EV wireless charging standards including SAE, ISO, and GB. Automakers and Tier 1 suppliers look to WiTricity to help accelerate the adoption of EVs by eliminating the hassle of plug-in charging and setting the stage for future autonomy.
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As part of the Global Oncology Products and Pipeline Strategy team, you will report to Vice President, Global Oncology Products & Pipeline Strategy and work with Global Business Development (GBD), Center for External Innovation (CEI), New Products Planning (NPP), Oncology Therapeutic Area Unit (OTAU), and Oncology Drug Discovery Unit (ODDU) to evolve and drive Takeda Oncology BD goals and strategy.
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As a part of the global project team, the successful applicant will contribute to the development of clinical protocols, provide scientific and technical support for regulatory communications and filings, as well as define the strategy for clinical endpoints and develop serology, mucosal/ cell mediated immunogenicity, efficacy-supporting diagnostics, and next generation sequencing endpoints for a late stage program.
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As a key member of our New England Water team, you’ll have the chance to work on challenging projects as the Sr Project Manager for water/wastewater treatment and conveyance projects – planning, directing, and monitoring all aspects of projects with increasing degrees of technical complexity from the concept stage through detailed design, construction services, and commissioning.
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The department offers B.F.A. degrees in Theatre Design/Technology, Stage & Production Management, Musical Theatre, Acting, Theatre, Theatre & Performance, Theatre Education, and Theatre Education & Performance.
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Process Development Senior Scientist, Late-Stage Drug Product Development. In this vital role you will work as part of a group that is responsible for late stage drug product formulation and process development for biologics modalities ( e.g. monoclonal antibodies, bispecific T-cell engagers ( BiTEs ), and fusion proteins.
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The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
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A global pharmaceutical manufacturing company located in the Boston region is looking to add a skilled Principal Scientist to their chemical development team. This individual will need to have expertise in oligonucleotide chemistry and process optimization in both early and late stage.
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Junior Software Engineer - Remote (Global), Full-Time. Entrepreneurial mindset - you have a proactive attitude, enjoy freedom and autonomy and act as an owner Fluency in English (French is a plus) Desired experiences: Early stage, SaaS and/or large scale publishing companies, min 3 years relevant work experience.
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Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
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Propose and implement global CMC regulatory strategies and provide regulatory guidance to cross-functional teams and functional areas for assigned programs from the pre-clinical stage through approval and life-cycle management.
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Funded by globally leading investors in the techbio field: Merck Global Health Innovation Fund, Accel, Mass Mutual Ventures and Mercia. 1-3 years of experience in a drug discovery or early-stage drug development environment.
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You will be responsible for managing the preparation and submission of high quality domestic and global regulatory submission documents (i.e. IND, CTA, NDA/MAA), as well as the development of response strategies to regulators, including liaising with regulatory operations to support submissions.
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stage global jobs in Boston, MA
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