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The Global Public Policy team's work spans a broad and diverse range of functions and workstreams, including government affairs and government relations; policy, product, and issue area expertise; risk and crisis management and mitigation; outreach, coalitions, and partnerships; and philanthropy.
$142,880 - $252,700 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Product Sales Regulatory Compliance:Adheres to compliance of Centers for Medicare and Medicaid Services (CMS), California Department of Health Care Services (DHCS), and L.A. Care's Regulatory Affairs & Compliance regulatory guidelines.
$50,216 - $75,324 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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KEY RESPONSIBILTIES:Develop strategic direction for Pharmavite’ s regulatory affairs team to include creating functional strategies and specific objectives to support functional infrastructure and the organization as a whole.
$212,585 - $318,878Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Who You’ll Work With The Program Manager, Transportation Electrification will work under the supervision of the Director, Customer Programs and will work closely with CPA’s Customer Programs, Power Planning & Procurement, Customer Care, Regulatory Affairs, External Affairs, Strategic Accounts, and Marketing teams.
$133,814 - $192,690 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Partner with Government Affairs to help positively shape the legal and regulatory landscape. Experience in other areas of law such as employment law, regulatory law, privacy, corporate law, or litigation would be a plus, but is not required.
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Knowledge of the complex regulatory, development, and medical affairs requirements in cell therapy. Develop and execute medical affairs strategy and maintain collaborative relationships with internal stakeholders including Clinical Development, Regulatory Affairs, Business Development, Technical Operations, and other teams to achieve business goals.
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Experience communicating and interacting with audit and regulatory agencies, including exam management and other regulatory affairs. The Compliance Remediation Manager ("CRM") will partner with the RBC-US Chief Compliance Officer (CCO)/CNB Chief Compliance Officer (the "CCO") and the CNB Deputy Chief Compliance Officer (the "DCCO"), whom together will be responsible for ensuring successful remediation of the current portfolio of regulatory and internal compliance issues, as well as those that may arise in the future.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
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10-12 years of experience in regulatory affairs preferably in a cosmetic or personal care products company; additional experience in quality control is a plus. Work closely with cross-functional leaders to develop and implement an effective and efficient regulatory strategy for domestic and international sales of skincare and cosmetic products through a deep understanding of the competitive market landscape, regulatory / legislative initiatives, and product marketing strategy.
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One of our key mid-sized biotech clients is seeking a dynamic Senior Manager/Associate Director of Regulatory Affairs to become an integral part of their team. Bay Area Senior Manager/Associate Director Regulatory Affairs Opportunity.
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5-7 or more years’ experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. This Associate Director, Regulatory Affairs, will work in the Abbott Rapid Diagnostics Division.
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Team with business unit Regulatory Affairs Specialists (RAS) to provide regulatory support for new product introduction (NPI) and marketed products under MDD and MDR Regulation. As Principal Regulatory Affairs Specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies.
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In-depth knowledge of the Global Regulatory Affairs environment – Guidelines and legislation. · Broad understanding of the pharmaceutical business in general and of other relevant associated regulatory areas (e.g., Clinical Affairs, Medical Devices, Chemicals Regulations, etc.
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Lead and interface with team members (Engineering, Manufacturing, Regulatory Affairs, Quality Operations, Quality Validation, Supply Chain, and other technical disciplines) representing the respective validation elements, as applicable, to determine validation strategy and system validation requirements based on concepts of life cycle: user requirements, functional specifications, design specifications, commissioning and validation.
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Significant experience (typically 8-10 years) in compliance management, regulatory affairs, or legal roles within the financial services industry, with a demonstrated progression in compliance leadership responsibilities.
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regulatory affairs jobs in Los Angeles, Columbia, Missouri
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