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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 4 days ago - 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 13 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 16 days ago - UpvoteDownvoteShare Job
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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality management, project management, finance, business operations, research and development, biometrics, health economics and outcomes research or manufacturing.
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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.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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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.
$50 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The City of San José Energy Department seeks to fill one (1) full-time Marketing and Communications Manager (Public Information Manager) position in the Account Management, Marketing, and Public Affairs Division.
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This position does not have relocation AssistanceAt Thermo Fisher Scientific, each one of our 75,000 extraordinary minds has a unique story to tell. Knowledge of safety, environmental, and regulatory standards related to chemical manufacturing.
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A minimum of 6-10 years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment. A minimum of 6-10 years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment.
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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 Robotics and Interventional Solutions platforms, reporting to the Senior Director, HEMA for Energy/Endomech/Robotics, 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 the Robotics and Interventional Solutions platforms.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Sr. Director, Office of Medical Affairs (OMA) is responsible for the oversight of Shockwave Medical, Inc. (SWMI) scientific communications, the investigator-sponsored research (ISR) program, and for the management of medical information on Shockwave Medical products for internal staff and external healthcare professionals (HCP.
$310,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support continuous collaboration with analytical development, technical operations, manufacturing, QA, regulatory affairs, clinical development, and program management, as well as external vendors (CROs and CDMOs.
$255,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Senior Assistant Dean is also an essential member of the law school in supporting the work of the Dean, the Associate Dean for Academic Affairs, and the Dean's senior leadership team. Assist the Senior Assistant Dean for Academic Affairs and the Dean in faculty and staff salary planning, annual budget planning, and law school fiscal and financial processes.
$172,400 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Bachelor’s Degree in Life Sciences; Advanced degree(s) in biomedical science, medicine, nursing, clinical/mechanical engineering, regulatory affairs, or related fields. Relevant working experience in clinical evaluation, project management, technical/medical/regulatory writing experience, risk management, biomedical/clinical research, regulatory affairs, clinical/quality/R&D engineering, or other related experience.
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affairs job Title: regulatory affairs Company: Thermo Fisher Scientific in Santa Clara, CA
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