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Track animal care and sustainability developments in legislative/regulatory affairs across species (cage-free, animal medication/housing, etc.) Work alongside Coca-Cola corporate teams to identify issues, legislative, regulatory, and lobbying opportunities.
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On-Board Scientific is hiring a Nonclinical Regulatory Document and Scientific Writer based out of either New Brunswick, Lawrenceville or Summit, NJ! Qualifications: At minimum, a Bachelor’s degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs. + years of Regulatory drug development experience Experience with CTD documents and nonclinical study reports for submission to global regulatory agencies.
$57.78 - $62.5Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Mammoth BioSciencesOPPORTUNITYMammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
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Minimum of 10 years of experience within Regulatory Affairs (Oncology experience preferred) As a key member of the Regulatory Affairs leadership team, you will play a critical role in ensuring compliance with global regulations and driving the growth of our company.
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Under general supervision from the Cultural Affairs Division Manager, the Special Events Manager manages the development of comprehensive and innovative strategies and approaches for events, programs, and partnership that serve community needs and draw regional tourism.
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We want people to join our team in the role of External Affairs Coordinator with expertise in community outreach, marketing, and public relations. DCI Donor Services operates three organ procurement/tissue recovery organizations: New Mexico Donor Services, Sierra Donor Services, and Tennessee Donor Services.
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The Army public affairs specialist participates in and assists with the supervision and administration of Army public affairs programs primarily through news releases, newspaper articles, Web-based material and photographs for use in military and civilian news media.
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The Deputy General Counsel (DGC) will serve as a key member of the legal leadership team, assisting the General Counsel in overseeing the company’s legal affairs. Provide expert legal advice on a wide range of matters, including corporate governance, regulatory compliance, mergers and acquisitions, intellectual property, and contract management.
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The Curriculum Manager works under the supervision of the Director of Curriculum within the Office of Educational Affairs (OEA). Overview The (OEA) at Tufts University School of Medicine is primarily responsible for the medical school academic programs, curriculum design and delivery, system-wide evaluation, faculty development, interaction with the offices of Student Affairs, Registrar, and Professional Degree Programs, and promotion of academic excellence through grant participation for innovative programs.
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The Counsel position will be an integral part of the Regulatory, Operations, Government Affairs and Environmental team. The Counsel will assist the Deputy Chief Counsel and Principal Counsel on various transactional, operational and regulatory legal matters primarily for Disney Signature Experiences (with a focus on Disney Cruise Line) and also the Walt Disney World Resort.
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Executive Director, Advertising & Promotions Regulatory Affairs at Bausch Health in Pocatello, Idaho, United States Job Description Bausch Health is a global company that develops, manufactures, and markets a differentiated product portfolio across multiple high-growth therapeutic areas including Gastroenterology, Generics, Neurology, Ortho Dermatologics, Medical Aesthetics and Dentistry.
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In addition, the incumbent is the key regulatory contact for Quality, Medical Safety and International Regulatory Affairs colleagues. Coordinates across the Allergan Aesthetics portfolio with the regulatory teams of each portfolio to provide consistent strategies for broad regulatory issues such as digital health t echnology and clinical outcome assessments.
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The Senior Regulatory Affairs Specialist (Sr. RAS) develops and executes strategies for global regulatory approvals working with Medtronic Geography Regulatory partners, and global regulatory agencies to introduce Mechanical Circulatory Support (MCS) product changes to market.
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Partner with the Regulatory Examination Project Manager to escalate and resolve any issues. Qualifications You Will, under the direction of the Lead Regulatory Licensing and Examination Manager: Manage an examination program that fulfills our legal and regulatory responsibilities, while endeavoring to minimize business and product impact.
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You’ll be engaged in projects dealing with International tax, mergers and acquisitions, state and local tax accounting, regulatory processes, tax reporting and strategy. Real Estate: Advise clients on their federal, local and overseas tax affairs, while acting as a strategic consultant related to: deals and transactions (including mergers, acquisitions and investments, conversions, reorganizations, dispositions, joint ventures, fund formation and structuring, etc.
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regulatory affairs jobs Title: account manager Company: Honeywell in WI, Germany
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