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Just-Evotec Biologics is seeking a Director/Sr. Director of Regulatory CMC to join a fast-paced, collaborative and multi-disciplinary team to lead all aspects of regulatory affairs for the advancement of low-cost biotherapeutics manufacturing.
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Serve as project manager for regulatory, environmental, and permitting projects and function as a task leader on larger projects. Primary responsibilities will be to provide support to a team of regulatory experts, scientists, and engineers to prepare hydropower licensing, permitting and compliance documents, perform consultation with agency and stakeholder groups, and support project management activities in accordance with Federal Energy Regulatory Commission (FERC) requirements.
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Coordinate with other privacy, compliance, and risk management leaders in the company to ensure our programs are aligned, as well as staying connected to governance owners, including Privacy Regulatory Affairs and Corporate External Legal Affairs Front Line.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Vendor Strategy Category Director will serve as the single point of business accountability in Clinical Development and Operations to support strategic sourcing, vendor selection, assessment, onboarding, and monitor performance of vendors in Oncology Regulatory and Medical Affairs Strategy.
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As The Focus Of This Internship, We Would Like To Study The Potential For How Generative AI Can Be Used In The Drug Development Lifecycle To Accelerate The Approach To Areas Such As Regulatory Filings, Generation Of Real World Evidence, Clinical Trial Documentation And Audits.
$10,120 - $12,170 a yearInternExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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You will lead business critical new product development projects, provide regulatory oversight to maintain lifecycle ensuring that the state-of-the-art requirements are maintained; Develop regulatory strategies and communicate risks within regulatory strategies vs project plan, and outline proposal for balancing the project risk to project teams and Regulatory Affairs Management.
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The Scientific Affairs Manager is a key member of the content development team who utilizes their combined skills as a scientific medical writer, educational design innovator, and grant development specialist to conduct a turnkey process that includes educational grant development, followed by content development for awarded grants.
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To that end, the US Government Affairs (USGA) team is looking for a Program Manager to assist members of the State Government Affairs (SGA) Industry team by providing related programmatic support and project management.
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Director of Government Affairs and Public Policy Modern Hydrogen Woodinville, WA - Full Time – Remote We are seeking an accomplished, enterprising government relations leader with over 15 years' experience driving policy transformations through bipartisan political channels and public-private partnerships.
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Regulatory Compliance:Stay abreast of regulatory changes and requirements relevant to proprietary trading operations. - Trade Processing and Settlement:Assist with the accurate and timely processing of all trades executed by the trading desk, ensuring compliance with regulatory requirements and internal policies.
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The Disability Resource Center reports to the Dean of Student Support in the Student Affairs division. Record all time on test proctor forms and within AIM MyDRC database. Follow test proctor forms for accommodations and faculty instructions.
$39,624 - $52,596 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our client is an environmental consulting and construction firm that designs and implements sustainable environmental solutions, including solid and hazardous waste management, landfill gas, site remediation, renewable energy, and regulatory compliance.
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Serves on internal project teams to shape the direction and influence actions based on extensive knowledge of regulatory requirements, industry standards, company strategy and laboratory technical implications.
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This candidate will primarily assist with regulatory compliance efforts for federal, state, and local environmental projects in CDM Smith’s portfolio, with focus on fisheries science, protected species, floodplains and wetlands, stream and habitat assessments, and associated permitting tasks.
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The Sr. Regulatory Affairs Specialist assists with development, management, and implementation of regulatory strategies to support new and existing Class I and Class II ophthalmic medical devices.
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regulatory affairs jobs Title: regulatory affairs project manager Company: Anthem in Redmond, WA
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