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A minimum of 6-10 years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment. The ideal candidate will have experience in chemical and environmental regulatory compliance, packaging regulations, product stewardship and industrial risk management in the medical device or manufacturing industries.
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The Regulatory Affairs Specialist- Contractor will assist or lead a variety of regulatory tasks in support of global regulatory strategy, regulatory assessment for modified product, regulatory filing for new/modified product, regulatory operation and processes, post-market surveillance.
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Bachelor's degree in Public Policy, Regulatory Affairs, Environmental Science, or a related field (Master's/MBA preferred). Demonstrated success in a regulatory affairs, public policy, or related role.
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Experience working with govt affairs, and other trade and regulatory bodies within Cisco and external to Cisco. Represent global manufacturing operations and supply chain in multidisciplinary govt affairs and trade team conversations where applicable.
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Minimum of 2-3 years of experience in quality assurance or regulatory affairs roles within the medical device industry, with specific experience in DHR review and documentation. Stay current with changes in regulatory requirements, industry standards, and best practices related to DHR documentation and quality management systems in the medical device industry.
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You will be responsible for managing all Regulatory Affairs activities (nonclinical and clinical) for investigational drug-device combination products from preclinical candidate designation through product approval, including regulatory submissions.
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Preferred Qualifications Experience working with legal counsel on regulatory and legislative affairs. The Virtual Power Plant Policy Director will lead SUN’s policy, regulatory, and advocacy efforts to implement solar + batteries Virtual Power Plant (VPP) policy across the country and in targeted states.
$80,000 - $90,000RemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Currently seeking a new senior director of regulatory affairs to lead and execute all FDA Pre-Market Approval submission activities as well as post-market supplements and international product registrations.
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Support Regulatory Affairs with relevant submissions, approvals, requests, and inquiries. Maintain trained status for, and comply with all relevant aspects of Noah Medical Quality Management System to ensure product and support regulatory compliance.
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The technical Writer will work closely with cross-functional teams, including Engineers, Scientists, Regulatory Affairs and Quality Assurance, to ensure accurate and timely documentation is produced.
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Strong collaboration and partnership skills are essential, as this role requires working closely with R&D, Global Strategic Marketing, Product Marketing, Regulatory Affairs, Quality, and Finance.
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Our Global Privacy and Regulatory Affairs team provides key support for all of TikTok's innovative initiatives, state-of-the-art products, and integrated platforms servicing our global video market.
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The Director, Regulatory Affairs is a key strategist, responsible for developing regulatory strategy for the Endoscopy business unit and delivering Stryker’s best-in-class Visualization products to market in the United States, Canada, and Europe.
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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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Strategic management experience in one or more of the following: Management consulting, Business Administration, Strategic Planning, Trade & Govt Affairs. Develop and execute global regulatory strategies for manufacturing fulfillment across one or more programs.
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regulatory affairs jobs in San Jose, Greenland, Kansas
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