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Associate II, Global External Manufacturing, Small Molecule Drug Substance (DS) works to support uninterrupted supply of Gilead's clinical and commercial products through execution of manufacturing campaigns within our global external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations.
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With liquidity solutions, exclusive data and insights, a custody offering, and a vibrant marketplace, Forge's goal is to build the best-in-class technology infrastructure to power a global private market that is transparent, accessible and seamless for companies, their employees and investors.
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Company Overview:Omni Logistics is a global provider of air, ocean and ground services, including supplemental services for enterprises dependent on the efficient movement of high value freight.
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Schwan's Company, a U.S. affiliate of the global lifestyle company, CJ CheilJedang Corporation, is a leading U.S. manufacturer and marketer of quality foods offered through retail-grocery and food-service channels.
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We are currently searching for a Research Analyst/Senior Research Analyst to join the Templeton Global Macro group at Franklin Templeton Investments in San Mateo, CA. Templeton Global Macro has been a pioneer in unconstrained global fixed income investing for more than 35 years, beginning with the launch of its flagship Templeton Global Bond Fund in 1986.
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As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
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This individual will play a key role in leading business development activities and in the management of key strategic alliances with global pharmaceutical companies in precision medicine oncology.
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In addition, this role will be responsible for leading, facilitating and supporting US and Global processes for harmonizing and integration of stability-related activities and supporting various GMP Quality Systems.
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PlayStation offers a global hybrid office/remote working model Flex Modes which aims to combine the flexibility of remote working with the magic of in-person collaboration. We welcome and encourage everyone who has a passion and curiosity for innovation, technology, and play to explore our open positions and join our growing global team.
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Global experience supporting geographical requirements related to data privacy, compliance, and legislation (EU and APAC) In partnership with our Global TA Leadership team and People Analytics team, the HRDA consults with HR leaders to identify key questions, run accurate analyses, and support leaders to tell the story of Talent Acquisition.
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With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
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Acts as Subject Matter Expert (SME) for safety-related activities within Global Safety Database per /Roche SOPs. Reviews, evaluates, and verifies potential AE information during Preliminary Assessment (PA) to determine required action per internal policies and procedures and perform data entry of adverse event by timely completion of the case via Roche global safety database.
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A scientific degree with directly relevant professional experience in small molecule development, global CMC regulatory affairs and CMC technical areas of at least 16 years with a BA/BS or 14 years with an MA/MS, PhD, PharmD, or MD.
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The Clinical Trial Specialist (CTS) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Global Clinical Operations team.
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Significant track record in leading regulatory operations staff through major global submissions (NDA, MAA etc) Extensive knowledge of North American/Global submission standards (FDA, Health Canada, PMDA, CDE, EMA, ICH, GXP, eCTD, etc.
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global job Company: Crowdstaffing in San Bruno, CA
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