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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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The Area General Manager will oversee two boutique hotels; Hotel Lucent and Hotel Keen. Work with your team to oversee, direct and manage property operations of this unique property for optimum performance and continual improvement in these five Key areas: guest service, employee satisfaction and development, sales/marketing, property appearance, and profit/financial control.
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Experience integrating Supervisory Control and Data Acquisition (SCADA) software for Human Machine Interfaces (HMI) development, SCADA systems, and embedded instrumentation and control applications in a process plant environment.
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The Quality Control Specialist will join our Quality team to be a key player in all scientific and documentation aspects of product development, release, stability, and investigations in support of maintaining and improving processes within the CRISPRevolution Production Team at Synthego.
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This person will collaborate with all functions to manage a quality system to support the company's diagnostic assay development activities, ultimately resulting in systems that are both FDQSR compliant as well as CLIA/CAP compliant.
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1+ years of relevant experience in Quality Engineering, specifically Automation Testing, Test Framework development. As a Senior Software Quality Engineer in the Alluxio QA team, you will be responsible for various aspects of delivering the Alluxio project as a product into the hands of our users.
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A minimum of 10+ years' experience and ownership of strategic business partnering, talent development, talent acquisition, organizational development, talent management, total rewards, HRIS, and people operations ideally focused on the biotech, technology, pharmaceutical, or healthcare market.
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May have cross-functional leadership roles, participate in business process development initiatives or represent the company in industry consortia. The leader will also be responsible for ensuring the projects they are responsible for have a cohesive regulatory strategy that is integrated into Pharmaceutical Development & Manufacturing (PDM) Project teams.
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Synthego is a genome engineering company that enables the acceleration of life science research and development in the pursuit of improved human health. By providing both commercial and academic researchers and therapeutic developers with unprecedented access to cutting-edge genome engineering, Synthego is at the forefront of innovation, accelerating the development of truly engineered biology.
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Manage effective and high-quality working relationship with the Federal Transit Administration (FTA) and environmental resource agencies such as the State Historic Preservation Office (SHPO), United States Army Corps of Engineers (USACE), Regional Water Quality Control Board (RWQCB), California Department of Fish and Wildlife (CDFW) and others as needed.
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We are seeking a highly motivated and scientifically rigorous individual to join the preclinical translational biology and assay development team. Research Associate II, Bioanalytical Development (Contract.
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Experience with access control list (ACLs), VRF, Port Security, Traffic Shaping, Priority Queuing, Class of Service (CoS), and Quality of Service (QoS) We are committed to the 17 United Nations Sustainable Development Goals and continue to align our business strategies towards mininising environmental impact, and advancing economic and social progress.
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Acting as a one-man attachment to other special forces teams, these highly specialized Airmen are trained in a wide range of skills, including scuba, parachuting and snowmobiling, as well as being FAcertified air traffic controllers in order to establish air control and provide combat support on missions all over the globe.
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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
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Responsible for development, maintenance, education, and implementation of departmental policies/procedures related to medical physics, dosimetry, and radiation safety. Works at the clinic site (Texarkana,TX) in collaboration with the Cancer Care Leadership to ensure high quality and safe interpretation, delivery, operation, and monitoring of radiation safety policies, procedures, standards, and equipment for Radiation Oncology Services.
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quality control business development jobs Title: project manager it in Redwood City, CA
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