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Wuxi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies.
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The Laboratory Technician I performs cell culture and cell-biology based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs.
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This role reports to the VP of Content and will be part of a global team of content, operations and data enrichment leaders. Clarivate is home to leading life sciences and healthcare solutions including Cortellis, solutions for Real World Data, medtech, market access and commercialization and deep consulting services.
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The PMV organization provides innovative technologies and strategic support for development and commercialization of Genentech and Roche’s biologic portfolio, including standard monoclonal antibodies as well as complex immunoglobulin constructs, fusion proteins, and modified proteins such as antibody drug conjugates.
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The Position The Senior Manager – New Product Commercialization (NPC) and 5D will lead and execute strategic and tactical elements of commercialization of assets from T-3 years to launch in Rare Disease.
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Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages.
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You will also coordinate with Global and Medical functions on FASENRA and Tozorakimab's LCM programs in preparation for commercialization of late-stage indications. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process.
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Understands trends in healthcare and pharmaceuticals, aware of competitor strategies, knowledge of healthcare dynamics in the US and other major global markets, and understands key frameworks related to corporate strategy, R&D, commercialization, and business development.
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As the Senior Product Manager, Sexual Health, you will be working on highly visible projects within the molecular diagnostics business unit, and will be responsible for driving execution of the global brand marketing strategy.
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Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world.
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This position plays a critical role in product development, ensuring patient safety while enabling early product development decisions, product design direction, product approvals, and market launch for product commercialization.
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Research Partnership is part of Inizio Advisory, a trusted advisor for pharmaceutical and life science companies that turns science into strategy, supporting execution at every stage of the product and patient journey from early commercialization to launch and beyond.
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This position is part of the Energy+ Additive Manufacturing Business Unit and will be located onsite in either Cortland, NY or Deland, FL. The business unit leads the development and commercialization of innovative solutions enabled by AM technologies to drive the growth of Pall Corporation.
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Overview WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies.
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Prior exposure to and strong awareness of regulatory / market access / commercialization requirements. PhD degree in the related discipline with 10+ years of drug development experience, including experience in Global Program Teams and with dossier submission for new or supplemental indication.
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