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Provide support to the Global Regulatory Lead (GRL) for key CMC regulatory activities pertaining to a development product (e.g. attendance to VDT if required, CMC input for Global Regulatory Plan, etc) and to product registration to achieve on-time approvals of GSK Vaccines submissions for the asset(s.
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10+ years of experience working in one or more of these areas: structured finance, securitization, collateralized lending or Delta One product development, liquidity and trading preferably in asset management and/or sell-side investment banking or trading.
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The senior leader, Cardiovascular Medical Affairs will have a strong understanding of all phases of product development, including preclinical development, clinical trial management, market preparation and launch readiness, post-launch marketing, post-approval studies, regulatory affairs, GCP and manufacturing compliance.
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The successful candidate will lead and oversee formulation-drug product process development, tech transfer, and manufacturing with external development and manufacturing partners; in addition to leveraging Cerevel's internal formulation development capabilities as well as a growing array of analytical and physical characterization instruments.
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Cultivate and drive improvements to the Tempus assay development process. As an individual contributor, manage a cross-functional team of scientists, engineers, and others to drive the planning, design, and development builds of our RNA portfolio that facilitate clinical decision support.
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The position is responsible for product development, technology transfer and overall management of CMC activities related to ensuring robust development and reliable GMP supply of oligonucleotide conjugates and intermediates.
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The Digital Asset Product Manager will work on product development, management, strategy, and marketing of a range of Fidelity Digital Asset Managment’s (FDAM) crypto and digital asset investment strategies and products.
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The ideal candidate will have strong and successful experience in leading aggressive packaging design and process development which includes conceptualizing, prototyping, specifying, commercializing, and validating new packaged product introductions into high volume production, enabling packaging as a consumer and customer differentiator.
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B2B Outbound Sales Job Summary As a Sales Representative (Outbound), you will be responsible for generating monthly sales through outbound cold calling or lead generation which plays a key role in the growth and expansion of Comcast Business Services and its product offerings.
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The Business Development Representative (BDR) is responsible for generating new business opportunities by reaching out to potential customers and clients. Learning & Development: Growth is a big reason people choose to join our team.
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Reporting to the Executive Director and serving on the senior leadership team, the Chief Development Officer (CDO) is responsible for creating and implementing the American Repertory Theater (A.R.T.) at Harvard University's fundraising strategy and leading a comprehensive development program that ranges from membership levels to 8-figure capital gifts.
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Key Responsibilities of a Process Development Engineer: Design and development of equipment, processes, and control systems, used for production and assembly of cell encapsulation devices.
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The Respiratory Sales Specialist provides clinical and educational tools and programs to ensure successful understanding and application of the respiratory product line. The Respiratory Sales Specialist assists in the development and expansion of new and existing businesses through in-services, training programs, and their respiratory clinical expertise.
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The VP (Digital Platforms) will be responsible for overseeing teams of software platforms and providing leadership, vision, product strategy/roadmap and technology direction for the platform engineering organization.
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The QC Associate II will support cellular therapy product release testing within the QC analytical laboratory at our BaseCamp facility in Waltham. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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product development jobs Title: product associate Company: Rtx in Boston, MA
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