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The OpportunityThe Regulatory Affairs Manager will work out of either our Plymouth, St. Paul or Maple Grove, MN locations for our Electrophysiology division. This Regulatory Affairs Manager may analyze broad scope implications of changing regulations and guidance.
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Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC. Minimum of 4 years' experience working under a quality system or a related discipline (e.g., Regulatory Affairs, Project Management, Quality Systems, R&D, Post Market, Operation Management)Prior experience leading and/or managing others.
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Are you a regulatory affairs and energy policy professional with experience in the RTOs (PJM), FERC and State Commissions? The Senior Manager/Director of Policy and Regulatory Affairs will play a pivotal role in shaping and advancing our client's strategic initiatives across PJM and regulatory landscapes.
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The Native Affairs Outreach Director serves as a liaison to Senator Smith, and takes meetings, attends events, and works with federal, state, and local agencies and Tribal governments on all issues impacting Tribal Nations and urban Indigenous communities.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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The Impact Youll Make in this RoleAs a Regulatory Affairs Specialist (product stewardship) you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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Ten or more years of financial services credit review/credit risk management experience through: past work in credit/loan review, credit risk management, internal audit credit risk coverage, commercial loan underwriting departments at large banking institutions; regulatory agency credit review/credit risk experience; or credit review/credit risk experience at a large consulting firm.
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As a Regulatory Affairs Specialist (product stewardship) you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world.
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O Manage accurate and timely safety related regulatory reporting (AEs, SAEs, UADEs) per study and regulatory requirements including collaboration with regulatory affairs and clinical operations, or overseeing activities of third-party managing safety reporting.
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Provide legal expertise and advise on all legal topics including complex commercial and licensing transactions, media rights, government affairs/funding, privacy, intellectual property, FCC regulations, employment, and union matters.
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Principal Regulatory Affairs Specialist - Structural Heart And Aortic, Mitral And Tricuspid (Hybrid)
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Principal Regulatory Affairs Specialist - Structural Heart and Aortic, Mitral and Tricuspid (hybrid) Reporting to the Senior Manager, the Principal Regulatory Affairs Specialist will support Research and Development programs with early phase pre-market regulatory strategy development with a view through the full product lifecycle.
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Help drive system and product requirements to meet the regulatory and compliance requirements (like GDPR, ISO, ISA/IEC, SOC2, FedRAMP) Help drive system and product requirements to meet the regulatory and compliance requirements (like GDPR, ISO, ISA/IEC, SOC2, FedRAMP.
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Provide subject matter expertise (SME) and serve as a liaison to Hennepin County Veterans Services (CVSO), the MDVA Homeless Programs Office, and Veterans Affairs (VA) Community Resources and Referral Center (CRRC) staff regarding inspection results.
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The selected candidate will join a team of talented software engineers in the Dolphin Software Organization working on Dolphin’s web hosted imaging and practice management software, Dolphin Blue. The Sr. Software Engineering role will be inclusive of product and systems design, development, testing, changes and upgrades, regulatory compliance, and product and systems support and maintenance.
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regulatory affairs jobs Company: Careerbuilder Us in Arden Hills, MN
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