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Demonstrates thorough knowledge of FDA / EMEA standards and quality systems, and the interface with other functions like manufacturing, distribution and maintenance. Supports the maintenance and improvement of quality systems processes, as needed.
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As a Battery Hardware Technician, you'll:Guide installation and acceptance testing of new manufacturing quality sensing systems. Expand your knowledge of machine learning vision systems and capabilities for manufacturing quality control.
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Apex Systems is working with a Health Technology Team seeking a Clinical Research Data Manager to work with the digital health technology team to execute data quality reviews for digital health projects.
$80 - $90 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Within the Facilities Division of the Public Works Department, electricians perform a variety of skilled and technically complex tasks in the operation and maintenance of City facilities with essential functions that include installing, troubleshooting, repairing, and maintaining building electrical distribution systems, lighting fixtures, lighting control systems, motors, VFDs, EV chargers, generators, and transfer switches.
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Ensure data quality, metadata management, compliance, and consistency of master data across business systems (PLM, SAP, MES, and other systems) to achieve a scalable digital ecosystem.
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Use commercial and proprietary software to create high-quality 3D art prototypes as proof of concept for project functional and aesthetic goals. Experience with Unreal Lighting, Post, and Niagara Visual Effects systems.
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Duties/Responsibilities:- Calibration of dose meters (including dosimetric inter-comparisons for QA) and radiation equipment (accelerator monitor unit calibration) Beam data acquisition for treatment planning- Preparation of data for treatment planning systems Development/improvement of dose measurement systems and protocols and software for dosimetry purposes (including spreadsheets and databases)- Ensures compliance with Federal, State and organizational regulations for radiation safety.
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As a Senior Data Architect specializing in Data Discovery, Data Mapping, Data Modeling, Data Quality, Enterprise Information Model adoption, different types of Database Storage Systems involving relational, NoSQL, azure cloud data solutions, and Big Data Analytical Platforms, you will play a pivotal role in designing, implementing, and optimizing our data architecture artifacts to support advanced data initiatives.
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We are establishing commercial processes that require a solid practical foundation in standard bioprocess unit operations (e.g. bioreactors, chromatography, UF/DF, normal flow filtration, mixing and novel harvesting systems.
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Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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You will regularly collaborate with the Drive Systems Geartrain design team, Materials Engineering team, and broader Prototype Machine Shop staff to produce high quality drive systems components at the front line of engineering development.
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Monitor, track, and trend stability data and GMP quality systems and establish metrics. Develop, implement, and maintain GMP quality management systems, policies, and SOP.
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Aid layout designers in the layout process, applying your skills to achieve optimal placement, routing, PCB stackup, signal quality, manufacturability, and cost. Ability to define and develop test procedures and to perform design verificationSuperior written and verbal communications skillsWhat will set you apart:Experience designing for medical equipmentSignificant experience designing circuits for motion control systems with motor drivers and sensorsExperience with high power (multi-kW) power distributionFighting cancer calls for big ideas.
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Experience in Device Quality System, Design, Manufacturing and Testing, 21 CFR Part 820, DHF, DHR, DMR, and overall Device Regulations, CDRH and 510 k or PMA approvals are a plus. Ensure Quality compliance of manufactured drug substance, raw materials and drug product, labeling, package inserts, and packaging of.
$160,000 - $225,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Certifications such as CQE from ASQ, Six Sigma Green Belt, certified Quality Systems Auditor. Experience in New Product Introduction (NPI) creating and improving quality systems.
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quality systems jobs in Redwood City, CA
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