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Johnson & Johnson is recruiting for a Principal Scientist, CMC Regulatory Affairs to be located in Raritan, NJ; Titusville, NJ; Horsham, PA; Malvern, PA or Spring House, PA. The Principal Scientist, CMC Regulatory Affairs provides support for the registration activities for a diverse portfolio of biologic drug products.
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The candidate will have a deep understanding of CMC regulatory frameworks and manufacturing with strong advocacy skills, experience with networking and a proven track record in the biopharmaceutical industry.
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The Associate Director (Associate Principal Scientist), Organon Manufacturing & Supply (OMS), Chemistry, Manufacturing & Controls (CMC), Network Project & Resource Management will provide regulatory CMC support, for Organon Network Projects.
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Forklift Operator Warehouse Laborer Forklift Driver Material Handler Warehouse Associate Warehouse Worker Forklift Technician Logistics Operator Inventory Specialist Warehouse Loader Distribution Center Worker Order Picker Shipping and Receiving Clerk Pallet Jack Operator Warehouse Equipment Operator.
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The Cyclotron Engineer functions as part of a team of peers to provide service and maintenance to cyclotron and radio chemistry synthesizers to ensure maximum productivity and system Up Time while utilizing time and resource management techniques effectively.
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Develop effective collaborations with research project leaders and projects team members, including biostatistics, regulatory affairs, clinical pharmacology, clinical scientists and development operations.
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We aim to help our clients solve their most pressing data management challenges by bringing key stakeholders together and helping them to navigate challenges such as cloud migration, implications of new technologies, evolving data sources, and pressure due to time constraints or regulatory requirements.
Full-timeRemoteExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Interact with CMC regulatory affairs personnel to gain knowledge on timelines and resource needs across the biopharmaceutical portfolio. Have experience in the biotechnology environment and a strong desire to learn about the biopharmaceutical development process and regulatory affairs.
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Supports review committees for medical affairs input and review, partnering closely with Regulatory, Legal and Healthcare compliance. The Executive Director of Medical Affairs US will oversee the Medical Science Liaison (MSL) team in the United States and will play a key role in developing and fostering relationships with the US KOLs, academic, institutional and governmental authorities in collaboration with the Commercial organization.
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The assistive technology specialist works at various types of program sites in the field with some time also spent in the office. Assistive Technology Specialist Credential. The Assistive Technology Specialist is a valuable member of a multidisciplinary team that provides support to individuals with disabilities through the use of assistive technology.
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At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Maintain accurate records of all dispensary activities including customer records, sales, deliveries and returns in accordance with the state regulatory agency and the standards set by Company.
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1035 Public Affairs Specialist. 1084 Visual Information Specialist. 0950 Paralegal Specialist. 0526 Tax Specialist. 2210 Information Technology Specialist. 1001 Digital Engagement Specialist.
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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The Sarbanes-Oxley (SOX) Control and Compliance Manager will lead the Company’s internal controls program, perform regulatory compliance audits as needed, and support the Company’s Environmental, Social and Governance (ESG) and Enterprise Risk Management (ERM) programs.
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The Group Fitness Instructor is responsible for consistently meeting daily class attendance goals as well as effectively promoting Life Time programs, products, and services. As a Group Fitness Instructor at Life Time, you have the opportunity to instruct a variety of group fitness formats.
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regulatory affairs specialist time jobs in North Wales, PA
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