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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
$100 - $113 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Our Client, the pioneer of and global technology leader in robotic-assisted surgery has a Regulatory Post Market Surveillance opening in Sunnyvale, CA. Escalating complaints to the Regulatory Post Market Surveillance Manager when new failure modes are encountered.
$38ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Regulatory Affairs Project Manager. Regulatory operations: BUDI number updates, label reviews, FDA laser report, state manufacturing license etc. On market support: regulatory impact assessments, etc.
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In this role you will be responsible for supporting and advising Apple’s engineering, product marketing, and government affairs teams on a wide variety of matters related to AIML products and policy, including research and publications, feature development, intellectual property, technology and content licensing, and regulatory proposals and compliance.
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Advanced degree such as MS or PhD in scientific/bioengineering field with 8-12 years of experience in Regulatory Affairs. The purpose of the Director of Regulatory Affairs, Imaging Agent Drug Development is to lead cross functional teams in major regulatory submissions to the Center for Drug Evaluation and Research (CDER), inclusive of New Drug Applications (NDA), End of Phase (EOP) Type B meetings, health authority interactions, label discussions, and securing approvals as part of an effort to bring small molecule fluorescence imaging agents to market.
$176,800 - $312,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Develop and drive meaningful public affairs campaigns that support Snap’s business goals. The Company’s three core products are , a visual messaging app that enhances your relationships with friends, family, and the world; , an augmented reality platform that powers AR across Snapchat and other services; and its AR glasses.
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QA Lead Software and Regulatory - Kohler Ventures. Support regulatory agency inspections in concert with the Kohler Ventures Management Representative in all functions and capacities. The ideal candidate will have a successful track record for working on regulatory and software lifecycle management methodologies for products related to health and wellness and mentoring technical professionals on these requirements.
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Our client is currently seeking a Regulatory Affairs for a 12 month + contract. Knowledge of regulatory guidance documents (FDA, Health Canada, EU MDR) for determining if a product change requires a regulatory submission (software and hardware devices.
$50 - $68 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This includes partnering with our security, trade compliance, and public policy experts to understand future regulatory requirements for which our supply chain processes remain subject to. This senior leadership role requires the individual to lead the development and implementation of our AWS supply chain regulatory strategy.
$141,600Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Summary: We are seeking a regulatory affairs specialist to assist and lead in the definition/implementation of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry.
$98,000 - $108,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Represent the bank by actively participating in outside civic/community affairs, business/ industry-related organizations and other professional activities as appropriate. Ensure regulatory compliance and staff adherence to bank policies and procedures.
$59,000 - $75,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are seeking a driven, creative, collaborative, and highly respected individual who is passionate about public policy, government affairs, regulatory policy, helping patients, innovative science, biotechnology, and public health to serve as Vice President, Policy & Advocacy.
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RA project team member for new quality system process changes and updates Education: Bachelor's degree required, Masters degree preferred Experience: Minimum of 3 years experience Skills: Knowledge of US and/or Canadian regulation relating to product and/or device clearance (FDA) Duties: Assists in definition/implementation of regulatory strategy and priorities in conjunction with management, peers, commercial, and affiliate personnel.
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You will be responsible for the development and maintenance of content and AI policies and supporting documents, and work closely with other teams within Google (e.g., Regulatory Affairs and Legal teams) on legal interpretation.
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Stay updated on relevant regulatory guidelines, industry trends, and best practices to contribute to continuous process improvement within the regulatory affairs function. Minimum of 5 years of overall related experience, with at least 2 years of industry experience within regulatory affairs project management.
Part-timeExpandApply NowActive JobUpdated 2 days ago
affairs job Title: regulatory affairs Company: Thermo Fisher Scientific in Los Altos, CA
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