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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 1 month ago - UpvoteDownvoteShare Job
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A solid grasp of art history, design history, photography and the visual arts, pop culture and counterculture, fluency in current technology and politics, and a deep understanding of the zeitgeist of social tastes and current affairs.
$205,420 - $287,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Assistant Vice President of Student Affairs, this role develops and implements strategies to increase job and internship opportunities, maintains strong relationships with employers at regional, state, national, and international levels, and collaborating with faculty, staff, and various university departments.
$67,000 - $77,000 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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These committees may be related to curriculum development, student affairs, faculty governance, or administrative decision-making. These committees may be related to curriculum development, student affairs, faculty governance, or administrative decision-making.
$105,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Demonstrated ability to effectively integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs. Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
$109,300 - $218,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.
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Collaborate with government affairs team to determine implications of sustainability-related policies and regulations, and translate them to action plans for Western Digital. Business Function: Regulatory Compliance.
$150ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Please note that not all roles are eligible to participate in the LTI program, and not all roles are eligible for equity under the LTI plan. Depending on your role and your performance, you may be eligible to participate in our annual Long-Term Incentive (LTI) program, which consists of restricted stock units (RSUs) or cash equivalents, pursuant to the terms of the LTI plan.
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The Regulatory Affairs Specialist III will manage activities associated with regulatory approval of in vitro diagnostic medical devices. Leading Pharma Company located in Pleasanton, CA, is hiring a contract Regulatory Affairs Specialist III with 5+ years industry experience.
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You will be eligible to participate in Western Digital’s Short-Term Incentive (STI) Plan, which provides incentive awards based on Company and individual performance. Lead Western Digital’s sustainability-related outreach to investors and shareholders in collaboration with the Legal Department.
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The Senior Regulatory Affairs Specialist is part of the team responsible for Core Business New Product Development with a focus on compliance to regulations from the US Food Drug & Administration (FDA) and the EU In Vitro Diagnostic Regulation (IVDR.
$103,500 - $170,800 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Title: Regulatory Affairs Specialist III. 5 years of experience in regulatory affairs in IVD or medical devices. Regulatory Affairs Certification preferred. Experience with regulatory submissions including IVDR CE submission, IDE, 510(k), and PMA submissions is preferred.
$55 - $70 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Serves as an expert resource to other departments Manufacturing/Operations, Quality, Marketing, Regulatory Affairs, Clinical Studies, and International Technical Services), provides timely response and follow-ups.
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Biotechnology company is hiring a Regulatory Affairs Specialist III to manage activities associated with regulatory approval of in vitro diagnostic medical devices. 5 years of experience in regulatory affairs in In Vitro Diagnostics or medical devices.
$56.73 - $75 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Category: Regulatory Affairs, Compliance, & Safety. Manage activities associated with regulatory approval of in vitro diagnostic medical devices. Provides support to currently marketed products, e.g., review engineering changes, labeling, promotional material, product changes and documentation for compliance and for changes requiring regulatory agency approval, as pertains to US and international regulatory requirements.
$56.73 - $75 an hourExpandApply NowActive JobUpdated Yesterday
affairs job Title: regulatory affairs Company: Beigene in Fremont, CA
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