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This is accomplished through cross-functional collaboration with internal groups including Clinical Development and Operations; Epidemiology; Regulatory Affairs; Medical Affairs; Commercial; and Global / Regional Market Access.
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Establish relationships with peers in key functions including MAM, Asset Strategy Leads, Pipeline Commercial Strategy, HEOR, Market Analytics and Insights, US Pricing, International Market Access and US Government Affairs, US Public Affairs, and US Medical Affairs.
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This position serves and provides direct support to the ID DVP Global R&D, DVP Global Regulatory Affairs, DVP Global Medical and Scientific Affairs, and to the Director, Portfolio Strategy and NPI Program Management Office.
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The applicant is expected to develop highly effective collaborations with relevant stakeholders including those in Patient Health & Impact, the Patient-Centered Outcomes Assessment Group, Statistics, Clinical Pharmacology, Clinical Development, Medical Affairs, Epidemiology, Programming, and other groups contributing to HEOR analysis and strategy.
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This new position will work closely with Global and Regional Market Access, HEOR, Marketing, Medical & Clinical Affairs, Research & Development, and Government Affairs colleagues to help ensure patients gain appropriate access to Abbott’s life changing point of care, rapid diagnostics.
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Engage with regulatory agencies and industry stakeholders regarding regulatory and legislative affairs, including by providing feedback on proposed regulations. 2+ years’ experience working in regulatory compliance or regulatory affairs for a consumer products, food, beverage, cosmetics or pharmaceutical company, or in a highly regulated industry.
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2-5 years' experience working in regulatory compliance or regulatory affairs for a consumer products, food, beverage, cosmetics, or pharmaceutical company, or in a highly regulated industry.
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Regulatory Affairs Associate (Food Science/Nutriti. Regulatory Affairs Associate. As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global.
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Responsible for talent development for the MMS-PA premarket Regulatory Affairs group; supervises and mentors RA associates. As Manager, Regulatory Affairs, you will provide leadership to the MMS -Pharmacy Automation platform team.
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Cell Therapy functions (CT Manufacturing Operations, Product Operations, Quality Assurance, Quality Control, CT Development, MSAT, Supply Chain, Finance, Regulatory, etc.) Demonstrated leadership & collaboration working in, or closely with, Supply Chain, GMP Manufacturing Operations, Manufacturing Science & Technology, Project & Program management, Quality Assurance / Quality Control Operations and related functions.
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Collaborate with other functions such as project management regulatory formulation manufacturing and quality control in project teams. Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to RD product development design and safety to ensure compliance in all research data collection and reporting activities.
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Regulatory Affairs Associate Abbott Park, IL. Job Summary: As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Provide overall oversight of school to ensure adherence with the Federal Head Start Program Performance Standards, ISBE Preschool for All/Prevention Initiative requirements, DCFS licensing guidelines, organization policies and procedures, and mandates from all funders and regulatory agencies.
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This position is located within the Captain James A. Lovell Federal Health Care Center in North Chicago, performing law enforcement work for the preservation of peace and the prevention, detection, and investigation of crimes occurring on Department of Veterans Affairs (VA) controlled property.
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The primary focus of this role includes proofreading and light editing for brand communications, public affairs and business writing. The proofreader will partner with creative directors, project managers, writers, senior designers, and at times, internal Client clientele.
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regulatory affairs jobs Title: regulatory affairs project Company: Gpac in North Chicago, IL
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