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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.
$113 an hourFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Kelly® Science & Clinical is seeking a Senior Regulatory Affairs Specialist for a 1-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology realm.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Senior Scientist I is responsible for oversight of the Scientific Affairs microbiology laboratory operations and performs laboratory investigations for on-market customer support. Oversee Scientific Affairs microbiology laboratory operations, including instrument maintenance, reagent and consumable inventory, SOP development and standard work sustainment and management.
$154,533 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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This role will manage the back-office operations of the global government affairs function. In this role you will also provide support to Alibaba IGA’s political compliance programs, including but not limited to the EU Transparency in Europe, and the Lobby Disclosure Act (LDA) in the U.S. This role will also provide other related administrative and logistical support for the Head of International Government Affairs for Alibaba.
InternExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Reporting to the Chief Operating Officer (COO), the Regulatory Services Program Manager will oversee regulatory staff and ensure services are delivered in accordance with Insignia’s standards.
$200,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Under general direction from the Regulatory Programs Division Manager, the Senior Environmental Engineer - Wastewater Treatment will focus on regulatory support to the Water Pollution Control Plant for NPDES discharge requirements and for air, safety, and hazardous materials compliance programs for the Plant.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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The Principal Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that products are developed, manufactured and distributed to meet regulatory requirements.
$151,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Together with the Associate Dean of Student Affairs and law school faculty, you will design and manage student programs and workshops that promote respectful and inclusive discourse, as well as address bias and enhance cross-cultural competency.
$139,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Cross functional partners include R&D, GSM, US marketing, Business Development, Medical Affairs, Clinical Research, Regional HEMA & Marketing, Regulatory Affairs, HCC and Legal. The Director, Health Economics & Market Access for the Wound Closure & Healing and Biosurgery platform, reporting to the Senior Director HEMA, will work in close collaboration with Global Strategic Marketing, Research & Development, Medical, Clinical & Preclinical, and Regional HEMA partners to build and execute fully integrated health economic and market access strategies for Wound Closure & Healing and Biosurgery platform.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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This role is expected to closely collaborate with multiple teams across Process Development, MSAT, Analytical Development, Regulatory Affairs, Quality and Manufacturing. Author and review plans, protocols, technical reports and CMC sections of regulatory submissions.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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As a member of the Global Medical Affairs team, the Senior Manager, Scientific Alignment will serve as a member of the US Legal, Medical, and Regulatory (LMR) review committee, reviewing US Commercial and Medical materials.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Minimum of 5 years of experience as a Developer/Business Systems Analyst with a focus on QMS in the medical device industry, including expertise in Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Collaborate with onshore teams and stakeholders to gather business requirements related to QMS functionalities, with a focus on Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
$92.59 an hourFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Stanford University seeks an accomplished leader to serve as Director of Human Resources for Student Affairs. Human Resources Director for Student Affairs. Participate in setting divisional objectives and goals, and design performance appraisal process for Student Affairs.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Parexel in Los Altos, CA
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