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Performs all functions of a legal professional employed as in-house counsel as directed by the Managing Legal Officer Intellectual Property, the Associate Vice President and Deputy Chief Legal Officer, the Vice President and Chief Legal Officer, and the Senior Vice President for Legal and Regulatory Affairs, including communications with clients, preparation of legal opinions, memoranda, documents, reports, and agreements as appropriate.
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Communicate regularly and effectively in a cross-functional matrix with development, origination, fundamentals, finance, and political & regulatory affairs staff to translate regulatory and market issues into business impacts and opportunities to benefit the position of Pattern's new and core business interests in MISO and other priority markets.
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Managing stakeholder engagement with the Equity Partner, LNG Offtaker and other internal teams such as Commissioning and Start-Up, Operations, Regulatory and Environmental, Feed Gas Pipeline, LNG Marketing, External Affairs and Community Relations.
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A chemical manufacturing company is looking to add a Senior Regulatory Affairs Specialist to their team. Prior experience in regulatory compliance is required, preferably in supporting a polymer production business, particularly polyethylene.
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As Director, Maritime Regulatory and Policy Affairs, you will lead all related requirements for Hanwha Shipping and play a pivotal role in supporting the expansion and development of our shipping business.
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Collaborate with cross-functional teams, including research and development, regulatory affairs, and manufacturing, to ensure successful formulation development and commercialization. Strong understanding of regulatory requirements and guidelines related to formulation development, including FDA and ICH guidelines.
$170,000 - $185,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Legal, Compliance, Regulatory and Government Affairs department is comprised of attorneys and other professionals providing high quality advisory and transactional support with integrity and objectivity across all parts of the organization.
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The Director of Public Affairs supports development and is responsible for execution of the Company’s legislative and regulatory agenda, as well as corporate brand positioning. Strong preference for at least two years of corporate experience in government affairs.
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The Senior Vice President of Clinical, Quality, and Regulatory Affairs manages providing the strategic direction and tactical management of all Clinical, Quality, and Regulatory Affairs functions.
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The Director ensures that all care management and population health processes seamlessly integrate with existing UM, Member Services, Quality Management and Provider Relations processes and are data driven and for development of metrics and measurement of program and member health outcomes for each of these areas and ensure programmatic compliance with all contractual requirements from HHSC, TDI, CMS, URAC and other regulatory bodies.
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. Description & Requirements In this role, they will support the Department of Veterans Affairs (VA) CSOC team, particularly focusing on the VA Enterprise Cloud (VAEC) security audit effort.
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Ideal candidate will have a degree in a discipline related to regulatory affairs with 5 years experience in a regulatory environment, or in quality systems with emphasis in regulatory submissions, supplier audits and will also oversee quality technicians.
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Additionally, the Senior Director is responsible for directing the strategy for the Medical Science Liaison team and other members of the HQ PN Medical Affairs to ensure appropriate evidence generation and communication plans with healthcare professionals.
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Proven track record of coordination with R&D, Operations, Finance, Marketing, Sales, Manufacturing, Executive Management, Quality Assurance, and Regulatory Affairs; ability to lead and drive stakeholder discussions.
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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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regulatory affairs jobs in Houston, IN, Pennsylvania
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