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We’re currently seeking a highly experienced Clinical Regulatory Leader, Health Authority Medical Review Team Lead, Master/Senior Medical Review Officer who is looking to draw upon their wealth of experience in clinical trial design and drug development to join Parexel’s highly recognized Regulatory Strategy team.
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A Bachelor’s Degree in planning, civil engineering, or a related field and 3-5 years of experience is required with an emphasis in the transportation planning field, actively engaging in general plans, specific/master plans, zoning code updates, public involvement, and regulatory compliance for a variety of client projects relating to equitable transportation development and construction, transportation demand management, mobility planning, multimodal access, surface transportation, and funding.
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Extensive knowledge of permitting/regulatory requirements in Iowa and/or Illinois. Bachelor’s degree in Civil, Environmental Engineering, or a related field. Ensure QA/QC measures are completed.
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Maintain agency and regulatory approval status (UL, CRN, ASME, KHK, CE, etc.) Stay abreast of emerging technologies & maintain technical competency in relevant subject matter areas via industry relationships, professional associations (ASHRAE, AHRI), and technical publications to maintain awareness of basic research activities, materials or processes, working fluids, regulatory implications, & supplier or competitive actions.
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Experience in implementing Analytics & Reporting solutions like Data Warehousing, Business Intelligence etc for enterprise applications, compliance/regulatory reporting etc. Finance, Compliance/Regulatory, Risks, HR, Supply Chain.
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Senior Regulatory Affairs Specialist - Electrophysiology page is loaded Senior Regulatory Affairs Specialist - Electrophysiology Apply locations United States - Minnesota - Plymouth United States - Minnesota - St. Paul time type Full time posted on Posted 3 Days Ago job requisition id 31080311 Abbott is a global healthcare leader that helps people live more fully at all stages of life.
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Support product launches in partnership with Quality, Regulatory, Operations, Marketing, Sales & Clinical Training. Ensure all quality system, regulatory, legal, and business requirements are met in the course of product development and market delivery.
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Develop and implement relevant Project Delivery, PMO, and CMO controls to ensure compliance with external stakeholders and regulatory bodies. Work alongside the Construction Management Office (CMO) and Project Management Office (PMO) to ensure key functional initiatives are met, including timeline adherence, budget control and quality management.
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The Regulatory Affairs Specialist will support international registrations and renewals. Laborie Medical Technologies is currently searching for a Senior Regulatory Affairs Specialist to join our team.
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The successful candidate will maintain a strong working knowledge of regulatory compliance regulations and International (ISO/EN/FCC/ICES/SAE/MilStd/RTCA) and Customer/OEM specific specifications, OEM product standards.
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Partner closely with Sherwin-Williams Legal department on regulatory applicability interpretations for products sold to consumers. -CONTINUOUS IMPROVEMENT Lead development of business requirements for any new or enhanced IT systems to support regulatory compliance for Sherwin-Williams products sold to consumers.
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We serve customers in more than 180 countries, operating through four divisions: Health; Tax & Accounting; Governance, Risk & Compliance; and Legal & Regulatory. Every day, our customers make critical decisions to help save lives, improve the way we do business, build better judicial and regulatory systems.
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Responsibilities also include treasury management, covenant modeling and compliance, regulatory compliance as well as corporate tax. Assist with the development and maintenance of policies and procedures for regulatory compliance and business activities.
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Support all company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirement. Experience with design controls, FDA regulation, GMP, GDP and QMS requirements.
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Familiarity with regulatory affairs, including OSHA (Occupational Safety and Health Administration), EPA (Environmental Protection Agency), and state agencies strongly preferred. Familiarity with ASME Codes, including Boiler Pressure Vessel codes and B31.3.
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grievance regulatory jobs in Minneapolis, MN
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