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Basic Qualifications: Master’s degree & 2 years’ directly related experienceBachelor’s degree & 5 years’ directly related experience Preferred Qualifications: 5-7 years in a Quality Control laboratory environment (GMP environment) within a commercial setting.
$122,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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SLs Specific Custom Scope (Primary Care, Medical Specialties, Dermatology, Pulmonology/Allergy/Critical Care Medicine, OB/Gynecology, Ophthalmology, Otolaryngology, Plastic Surgery, Urology, Psychiatry/Behavioral Sciences, Pain Management)Develops and coordinates the creation of the SLs quality plan that aligns with organizational quality goals.
$94.28 - $124.9 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The VMI shall ensure compliance with all applicable regulations which may include, but are not limited to: Annual permits, Encroachment permits, Traffic Control Plans, railroad permits, Caltrans permits, and environmental protection measures as documented on Environmental Release to Construction.
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The Commissioning Construction Manager will lead our commissioning quality control efforts onsite by assisting contractors with startup preparation. Experience with project management software such as Prolog, Procore, E-Builder, Bluebeam, Microsoft Project, and Primavera Project Planner (P6.
$160,500 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Adverums 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.
$70 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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R&D Quality is seeking an Executive Director, Head of Audit to join our Leadership Team that oversees GCP, GLP/GCLP and GVP activities at Gilead. Communicates audit information to relevant Gilead leadership and functional areas via management reviews and quality forums.
$323,070 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Independently author and lead quality records such as Deviations, Lab Investigations, CAPA, Change Control including leading thorough and timely investigation and/or implementation activities.
$78,915 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead best practices for Palantir Foundry development, including modularity, testing, version control, and continuous integration (CI/CD). Ensure data quality and governance through well-defined data transformation processes, testing trameworks, and documentation.
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Demonstration of outcome-oriented team leadership in some aspects of pharmaceutical manufacturing, or supply chain, or quality, or CMC regulatory, or process development, or as part of a cross-functional product team in the broader pharmaceutical industry.
$307,560Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are looking for a highly motivated, independent, and skilled Research Associate to join the Quality Operations team at Kodiak Sciences to work on antibody purification, characterization, formulation, and conjugation.
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What You will do:Develop schematics comprised of FPGAs, SoCs, memories, communications devices, analog devices, ADCs, DACs, motion control devices, feedback sensors, power supplies. Aid layout designers in the layout process, applying your skills to achieve optimal placement, routing, PCB stackup, signal quality, manufacturability, and cost.
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Food & Beverage: Safety, Quality Control. Electronics, Power: Ionic impurities in High Purity Water and ReagentsSUMMARYReporting directly to the Director of Operations, Sunnyvale, CA, this position directs and coordinates activities of personnel engaged in Manufacturing Planning, Purchasing, Warehouse Operations, Inventory Control, Customs Compliance, Order Management of plant manufacturing operations.
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Dispatches fire, police, medical and animal control personnel and equipment on both routine and emergency calls utilizing a CAD system, multiple video display terminals, radio dispatching consoles and related equipment.
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Strong working knowledge of IVD and/or medical device development, design control, change control and cGMP / Quality Systems. Senior Regulatory Affairs Manager (Open to Remote, Hybrid and Onsite Options) Full-time.
$177,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Implement, evaluate, and maintain quality control standards to ensure program success. Members of the SSRL-ESD are responsible for establishing performance criteria, evaluating potential system designs, and implementing/supporting machine protection systems (MPS), personnel protection systems (PPS), beam containment systems (BCS), computing and networking infrastructures, beamlines data acquisition, and motion control systems while ensuring designs and installations are properly documented.
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quality control jobs Company: Ss C in Palo Alto, CA
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