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Analytics Insights, Business, Business Direction, Client Relationship Management, Finance, Global Market, Marketing Strategies, Portfolio Management, Regulatory Compliance, Sales, Structured Products.
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Work with Senior regulatory personnel / Manager to identify regulatory and product registration needs and requirements for new products. Responsibilities: The Snr Product Regulatory Specialist is responsible for obtaining registrations and certification approvals for new and existing products, necessary to sell them to worldwide markets.
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Regulatory Compliance : Support HEP’s ongoing compliance with federal, state and local regulations affecting the midstream oil and gas industry, including environmental and commercial regulatory compliance and coordinating outside regulatory counsel as necessary.
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Experience analyzing compliance with regulatory programsrelated to water, wastewater and/or air quality. For more detailed information, refer to the Regulatory Compliance Specialist job description.
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May develop Standard Operating Procedures (SOPs) and Work Instructions (WIs) as directed by the Senior Director CMC Regulatory Affairs. Prior pharmaceutical industry experience and a minimum of 8 years in CMC Regulatory Affairs for Associate Director.
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CCRP - Cert Clin Research Prof (Preferred) or RAC - Regulatory Affairs Cert (Preferred) 2 Years experience in a regulatory role or 4 Years experience in related clinical research role (Required.
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Work closely with NGS production, Quality and PreClinical Genotox for compliant execution of genotoxicity data packages in support of regulatory filings and clinical programs. Interact with Health Authorities, in writing and verbally, including pre-submission (e.g., pre-IND), scientific advice filings, IND or CTA, meeting briefing books, or other requests from global regulatory authorities.
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US Army Corps of Engineers (USACE) Office of the Chief of Engineers (OCE), responsible for the Army Nuclear Power Program, is ramping up to meet a wide range of operational, engineering, logistic regulatory certification and permitting requirements for future Operational Readiness Review (ORR) in accordance with Army Regulation 50-7 "Army Reactor Program" (ARP.
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Highly reputable, established, Fintech looking to appoint a Legal Counsel/ Financial Services Regulatory Counsel in NYC to expand their In-House legal and regulatory compliance capability/ team.
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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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We are looking for a regulatory specialist and permitting lead to support our clients in central and northern California. Work will include managing regulatory complexities and permitting for a range of projects, from municipal projects to large infrastructure programs, working with multidisciplinary teams of specialists, and performing both office and field work.
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Ensures all appropriate CMC regulatory aspects across teams to support change control requests including transfer of supply within GSK or with a 3rd party are delivered to agreed timelines. Scope of Responsibility·Will serve as a key strategic partner representing Global CMC Regulatory on Regulatory Networks and Matrix Teams, providing and overseeing strategic direction and guidance to Biopharmaceutical, Pharma Supply Chain, Clinical Trial Supply, Quality Assurance, and Commercial interfaces on both global project and key strategic business initiatives.
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Reporting to the Vice President, CMC Regulatory, CARGO is seeking an Associate Director, CMC Regulatory to help progress development of our cell-based gene therapy portfolio. 10+ years of experience working directly in regulatory CMC or in a relevant technical development discipline, such as process development, analytical development, or quality assurance, including at least 6 years' experience directly in CMC regulatory.
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First line operations manager of all activities at MercyOne Des Moines and a member of the pharmacy leadership team.
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As an integral member of Pharmacy Services, the IDS/Pharmacy Regulatory Coordinator's role also includes assuring accurate record keeping, filling, compounding and delivering of investigational drug products to study coordinators, study nurses and patients.
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Title: regulatory Company: International Trucks
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