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This position is part of the Regulatory Affairs Department located in Coralville, IA and will be remote. Process cross-functional requests for label initiation and design to meet regulatory compliance requirements of product intended uses.
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Youve got at least four years experience in the Life Sciences R&D industry in at least one of the following areas: research, clinical development / operations, pharmacovigilance, regulatory, medical affairs, medtech, patient services, MD&D (medical device and diagnostics) or related areas (CROs), health institutions, health technology companies, etc.
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The Product Safety Toxicologist will report directly to the Regulatory Affairs Director. We are seeking an experienced regulatory toxicologist as a Product Safety Toxicologist for our global Regulatory Affairs organization.
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Ensure compliance with applicable regulatory agency requirements, published standards, company policies/procedures, local procedures/work instructions, and project specific plans. Execute label and specification configurations within manufacturing BOMs, LIMS and other systems to ensure products are attributed to the appropriate labeling.
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Degree required (MS or MBA minimum) 10 years related clinical, quality, and regulatory affairs with a preference for M.S. or MBA equivalent. Ability to articulate clear visions and expectations for Quality and Regulatory Affairs.
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Preferred: Certification from the Society of Clinical Research Associates (SOCRA), Association of Clinical Research Professionals (ACRP), Research Administrators Certification Council (RACC), Certified IRB Professional (CIP) or, Regulatory Affairs Certification (RAC.
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Collaborate with cross-functional teams, including operations, engineering, land and regulatory affairs, to ensure alignment and integration of health, safety, environmental, and regulatory requirements into business processes and decision-making.
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Incorporate awareness of relevant trends in EV markets, public policy/regulatory affairs, and utility tariffs to help build and lead execution on integrated EV charging commercial strategy.
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Tallgrass Energy is currently in need of one Regulatory Affairs Specialist to join our Houston based Capital Projects Team. This role will report directly to the Director of Environmental permitting, or other Leadership as assigned within the Capital Projects - Environmental & Regulatory Department.
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Collaborate with cross-functional teams including R&D, Quality Assurance, and Regulatory Affairs to ensure comprehensive validation coverage. Strong understanding of regulatory requirements and guidelines (e.g., FDA, GMP, GLP) related to IVIS validation.
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Regulatory Lead serves as a subject matter expert and enterprise-wide coordinator of regulations promulgated by the Bureau of Land Management, Bureau of Indian Affairs and state oil and gas commissions.
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The Senior IGA Specialist reports to the Director of Legislative Affairs and Funding Opportunities of the Harris County Intergovernmental and Global Affairs Department. Five (5) years of experience working in a public policy or government affairs related capacity with progressively increasing levels of responsibility.
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Airswift is looking for a Regulatory Lead to work with a major Oil and Gas company on a initial 6-months contract (with the possibility of extension). The selected candidate will primarily be focused on rolling out regulatory rules internally at MRO. This person will act as the Project Lead for implementation of federal rules across stakeholder groups.
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7-10 years of experience supporting environmental regulatory permitting and compliance in Upstream Oil and Gas. Demonstrated ability to move projects through complex environmental regulatory and permitting requirements while addressing project cost and schedule implications in a dynamic and fast paced working environment.
$100 - $135 an hourExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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4 years of experience in the product industry with at least 2 years experience in quality assurance or regulatory affairs. Plan and perform independent audits to evaluate and determine customer’s quality systems and/or products compliance to applicable standards and regulatory requirements.
$100,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago
regulatory affairs jobs in Houston, IN, Pennsylvania
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