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Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for developing strategies to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to existing devices.
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Preferred Qualifications: Graduate degree in Toxicology or related field (Pharmacology, Public Health, Biochemistry, etc) Prior regulatory expertise with programs and agencies such as the U.S. EPA, FDA, OSHA and counterpart regulatory agencies outside the US. Past participation in industry or trade association consortia addressing toxicology and regulatory issues.
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Recruiter: Spencer Gregory Hale Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle.
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Job Summary:The Senior Associate is responsible for performing analysis, examination, review, assessment, and testing in a wide variety of client engagements at the direction of the project manager.
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Demonstrate expertise in BSA/AML and OFAC including: BSA/AML and OFAC laws and regulations as well having a some understanding and experience of how to apply requirements in financial service environmentCreative problem-solving abilities and ability to interpret information and regulatory requirements in order to advise clients on compliance issues by implementing sound solutions.
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The ideal candidate should possess a strong background in handling regulatory and compliance matters before the Texas Public Utility Commission, state energy regulatory commissions, and entities such as the Electric Reliability Council of Texas (ERCOT) or other ISO/RTOs or organized power markets.
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The Regulatory Affairs Specialist is responsible for assisting the St. Croix Hospice Legal Department by filing, maintaining, and tracking government licenses and supporting documentation, responding to routine inquiries related to licensing, and supporting strategic growth efforts to obtain licenses.
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Work with partners to independently develop and convene stakeholder engagement processes that are seeking to address utility regulatory issues towards reducing greenhouse gas emissions in the energy sector.
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Job Summary:The Senior Associate is responsible for performing analysis, examination, review, assessment, and testing in a wide variety of client engagements at the direction of the project manager.
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We have an exciting opportunity at Ameriprise as a Regulatory Affairs Analyst! This position is part of a team that provides day-to-day operational support to the Regulatory Affairs team in managing regulatory exams, inquiries and internal investigations.
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Prior experience at a major law firm, in-house legal department of a financial institution and/or bank regulatory agency. Knowledge of relevant regulatory agency rules and regulations essential to this position (e.g., OCC, FRB, CFPB, and FINRA.
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Experience in implementing Veeva Vaults (Quality, Clinical, Regulatory, Safety), LIMS, and/or Validation Lifecycle Management Systems. In addition, our team also works on projects with clients to manage these Quality business processes for supply chain, manufacturing, commercial operations and R&D. This includes analyzing various cGMP and 21 CFR Part 11 regulations in the Regulatory Compliance area to determine impact on risk exposure.
$82,800 - $136,600 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Quality IT Business Analyst is a key member of global IT with responsibility for functional requirements definition and configuration of systems supporting quality and regulatory capabilities (PLM, eQMS, CAPA, NC, RIM.
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What you need to have: FINRA Registrations Series 7 and Series 24 3+ years of financial services experience, preferably with an independent broker-dealer Prior experience with Regulatory Research Prior experience communicating with clients and writing client responses Bachelor’s degree #LI-Hybrid.
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Bachelors degree in microbiology, food science, regulatory affairs, or related discipline. 5+ years of experience with an ingredient/food manufacturing company or food science/technical/regulatory organization with specific time spent in international food safety standards and regulations.
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Title: regulatory Company: Clarivate Plc in St Paul, MN
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