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U00A0 S/he will lead the global Integrated Brand Teams (PKU and ERTs) with representation from Strategic Markets, Regions, Value and Access, Medical Affairs, Worldwide R&D, Supply Chain, and other key stakeholders to develop a cohesive, insights-based global brand strategy across the product life cycle.
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This position will require interaction with multiple levels in quality, Regulatory Affairs, Manufacturing, Supply Chain, Materials Management, and Contract Manufacturing Operations. Minimum 3-5 years of experience in a Quality, Compliance, and/or Regulatory setting.
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This position requires interaction with multiple levels in Quality, Regulatory Affairs, Manufacturing, Supply Chain, Materials Management, and Contract Manufacturing Operations. These individuals build and maintain the company's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
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Battery energy storage, microgrid and/or front-of-the-meter project development experience is preferred. Knowledge of energy project design and implementation of clean energy technologies, such as EV/EVSE, solar PV, battery storage, and microgrids.
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The La Vida Dominican Project Director works closely with the Vice President for Academic Affairs and affiliated faculty and staff of La Vida Dominican program and the Dominican campus to oversee and coordinate project activities and integrate holistic support services for students and community into Dominican planning and processes.
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Arcadis is seeking an Associate Project Manager with relevant experience and a background as a Geologist, Environmental Scientist, or Environmental Engineer to join our team. Field work may be performed at project sites with environmental media (e.g., soil, sediment, groundwater, surface water, etc.
$76,110 - $132,750 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A Associate Director, Regulatory Affairs , you. Associate Director, Regulatory Affairs. In collaboration with Regulatory Affairs functional management, coordinate the provision of resources from the various Regulatory functions in support of clinical studies.
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Nonclinical / Clinical Regulatory Affairs experience preferred. Ensure strategic alignment with the Clinical Development Plan (CDP) and nonclinical development plan with input from clinical and nonclinical Subject Matter Experts (SMEs), respectively, and regional regulatory leads.
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A scientific degree with directly relevant professional experience in global CMC regulatory affairs and CMC technical areas of at least 15 years with a BA/BS, MA/MS, PhD or PharmD. Lead the execution of global CMC regulatory plans, including overseeing the submission and approval process in close partnership with other functions in PDM, Regulatory Affairs, and Clinical Development.
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A valid certificate from a Department of Consumer Affairs Medical Board-approved agency to work as a Medical Assistant:American Association of Medical Assistants. California Correctional Health Care Services (CCHCS) is dedicated to enhancing public safety and promoting successful community reintegration through education, treatment, and active participation in rehabilitative and restorative justice programs.
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The Construction Project Manager will be responsible to logistically plan the sites, create and maintain schedules, manage bidding processes, award contracts and ensure all projects are delivered in time and within budget.
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We are seeking a Project Manager to manage projects and back-end logistics, including purchasing, coordinating project schedules with multiple vendors and clients, quality assurance, submitting color samples, and coordinating with shippers nationwide.
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Should have good working knowledge of all areas of development – including CMC, non-clinical, clinical, project management and regulatory functions. Will be responsible for project execution and on time delivery of milestones, managing outside partners and alliances, and facilitate meetings.
$160,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Responsible for all aspects of Project Administration including ensuring correct setup of new Projects; attending weekly job site meetings; delegating duties to Assistant Project Manager (APM), ensuring proper upkeep of all logs and documentation; and review of all outgoing correspondence related to assigned project(s.
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This is reflective in our competitive offerings to our hires including: Ongoing HR supportCompetitive benefits packages including- Health, Dental, Vision & Life insuranceOur very own JLM Rewards incentive programTHE IDEAL CANDIDATEThe ideal candidate has a proven track record of project engineering and civil construction work.
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affairs job Title: regulatory project Company: Jobget in Novato, CA
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