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Organize and coordinate non-clinical (CMC, Supply Chain) team activities and deliverables; manage weekly team meetings; prepare agendas and keep track of action items. Manage multiple CMOs to drive manufacturing activities in alignment with CMC timelines and clinical supply needs.
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Perform hands-on tasks such as building ion propulsion drone or assembling power supply prototypes. Design and build an ion propelled drone including the mechanical structure and the super-lightweight on-board power supply.
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Identify and collaborate effectively with key ICs and leaders across: FLOPS (Finance, Legal, Operations, People and Supply Chain) and more to solve key business challenges through implementing best practice solutions which can include process change, configuration, and/or customization.
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Collaborate with internal teams (Process Development, Quality, Regulatory, Supply Chain, and Commercial) and external partners (CDMOs/ CROs/ CTLs) to continuously supply qualified reference standards and critical reagents.
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Snowflake Exp Developer or Admin or Support with any cloud Experience with excellent process knowledge in any of the following areas: Finance, Supply Chain, Marketing, Sales, and Customer Service.
$250ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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2+ years of experience designing and implementing mixed-signal circuit boards from concept through production using processors, FPGAs, Ethernet, multi-GHz Serdes, DRAM interfaces (DDR4), I2C, SPI, PCIE, RF-sampling ADCS/DACs (or RF transceiver modules), and power supply components.
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Such as supply and demand management, Ads network connection and marketplace, creative lifecycle, inventory management, bidding and optimization solutions, data exchange, tracking, measurement and reporting capabilities.
$200ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collate manufacturing process data to develop metrics, control charts and reports to improve manufacturing processesAssist with Supply Chain, Analytical, and Stability activities as neededReview/approve documents associated with Drug Product development and manufacturing, such as change controls, manufacturing batch records, protocols, investigations/deviations, and reports, and organize and archive documents in Veeva Quality Docs System.
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Represent Global Regulatory Affairs on the Global Artwork Team; help develop, review, and approve global package artwork in close collaboration with Supply Chain, Quality Assurance, and International Regulatory Affairs colleagues.
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Our projects span various domains, including Connected Vehicle, Smart Mobility, Operations, Manufacturing, Supply Chain, Logistics, and Warranty Analytics. Ford's GDI&A department is on the hunt for talented individuals skilled in Machine Learning, Big Data, Statistics, Econometrics, and Optimization.
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Experience with writing, developing, maintaining product labeling in the US and EU is required and around the globe is desirable including Asia-Pacific, LATAM, and Middle East. Experience with using Veeva Vault RIM and QualityDocs is desirable.
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The service members of the Purchasing, Supply & Logistics community make sure America’s Navy has what it needs, when it needs it. Officer positions in the Supply Corps are available to college graduates, and Logistics Specialist (LS) positions are available to those without a degree.
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Kirra Services is a Supply Nation Certified ICT Service Provider. Aruba Certified Mobility Associate (ACMA) Aruba Certified ClearPass Associate (ACCA) Cisco CCNA – Routing and Switching. Kirra Services is a Supply Nation Certified ICT Service Provider.
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5-10 years of FP&A, Strategic Finance or Operational Finance experience in a technology company involving hardware, manufacturing operations, supply chain, and logistics. Skydio designs, assembles, and supports its products in the U.S. from its headquarters in Redwood City, CA, to offer the highest standards of supply chain and manufacturing security.
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Liaise with functions such as Development, Manufacturing, Supply Chain, Project Management, QA, QC, and Regulatory Affairs as well as off-site functions such as external partners. We believe that our PCVs could receive regulatory approval based on successful completion of clinical studies utilizing well-defined surrogate immune endpoints, consistent with how other PCVs have obtained regulatory approval in the past, rather than requiring clinical field efficacy studies.
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supply chain jobs Title: emergency in San Carlos, CA
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