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Determines appropriate assays and vendors for clinical biomarkers, and manages outsourcing of biomarker assay development and validation partnering with Translational Sciences colleagues when applicable.
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A commitment to ethical scientific research and a passion for advancing the development of new treatments for cancer patients. Functional scientific knowledge of clinical pharmacology, pharmacokinetics and dynamics, interpretation of basic safety pharmacology and toxicology data, surrogate marker identification and application, PK/PD drug interactions, in vivo/vitro models and population pharmacokinetics and PK/PD modeling.
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Includes oversight of CT technology, process development, analytical development and testing, gene delivery and editing, and clinical supplies delivery. Ensure strategic alignment of technology and program development plans with key stakeholders/partners in R&D, Commercial, Regulatory and GPS. Serve as a member of the Cell Therapy Development Operations Leadership Team.
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The Associate Director, Healthcare Quality Improvement is a role within the Global Professional Relations and Independent Medical Education (gPRIME) team of Global Medical and Scientific Affairs (GMSA) that is primarily responsible for supporting Our Company’s collaboration with key external healthcare quality organizations and engagements with professional medical societies on ways to improve healthcare quality and guideline-concordant care.
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PSEG offers a unique experience to our more than 12,000 employees - we provide the resources and opportunities for career development that come with being a Fortune 500 company, as well as the attention, camaraderie and care for one another you might typically associate with a small business.
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BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream and Downstream Process Development & Engineering. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies.
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The Principal Scientist is a senior scientific role whose primary responsibility is to lead program-specific method development activities for therapeutic proteins in our company's biologics portfolio, from the discovery interface through first product registration.
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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.
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Experience in the legal fields of energy (including renewable energy, development, real estate and/or structured and project finance) LEGAL INTERN - Solar EPC, Development, & Energy Storage.
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Assist to train, coach and develop new peers on La-Z-Boy product knowledge and selling process/skills to achieve store sales goals. Consistently execute the La-Z-Boy selling process and strive to provide a favorable experience to all customers.
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The permit writer will leverage their technical expertise in the field of biology and environmental science to expedite the permit application process. Professional development opportunities.
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Curing: hanging and dry-racking flowers; monitoring curing process and climate control; labeling; weighing and inventory data input. Plant monitoring and care during vegetative and flowering phase: trimming and staking; big leafing and pruning; plant care, watering and feeding; plant monitoring and climate control; pest and disease control; inventory data input.
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Assembly process development experience. He/she should also have in-depth knowledge of metal and polymer 3D Printing process and design for additive manufacturing. Knowledge of Process Excellence (Lean, Six Sigma) and Risk Analysis tools/methodologies preferred.
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Deliver impactful outcomes by leveraging a deep understanding and experience in navigating typical workflows within drug discovery, drug development, gene-to-antibody, and proteomics. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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For the TWA Hotel at New York’s JFK Airport, MCR won the Development of the Year (Full Service) Award at The Americas Lodging Investment Summit (ALIS) , the Urban Land Institute New York Excellence in Hotel Development Award and the American Institute of Architects national Architecture Award, the highest honor given by the AIA.
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process development scientific jobs in Rahway, NJ
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