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Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of client.
$32 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum of 6 years of experience in drug safety/pharmacovigilance quality assurance or compliance within the pharmaceutical or biotech industry. Certification in pharmacovigilance (e.g., RQAP-GLP, PVQA) or quality management (e.g., ASQ Certified Quality Auditor) is a plus.
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Support the performance of the other appropriate Quality Assurance functions including document writing/revisions, deviations, CAPA's, document/data review and other administrative duties as needed.
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Demonstrated success with domestic and international consulting, permitting, licensing, and environmental quality review processes for a wide range of infrastructure projects in sectors such as power generation, process industries, water/wastewater treatment, telecommunications, data centers, and industrial manufacturing.
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Partner closely with Onyx’s cross-functional team of product managers, engineers, and data governance specialists to create and maintain high-quality, scalable, and secure computational data governance products tailored to meet the specific needs of enterprise internal stakeholders.
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Critical aspect of the role includes defining an agile quality and compliance strategy that supports Digital Data unit in their effort to establish a standardized, resilient, and sustainable data pipeline - including data sources, data quality, data governance, data management and master data management.
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We have already launched our own Enterprise Data Hub, the digital backbone of this company, and we need more engineers in the data analytics discipline who are forward thinking, self-guided and innovative to continue to build out the hub across our lines of business, integrating all of our data, mastering data and focusing on data quality to fundamentally shift the way Charles River operates through data science and advanced analytics.
$125,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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IT CSV project engineer's IT System Administrators and System Owners and Quality Assurance on projects including clinical data repositories master data management. Assess change controls for impact to validated computer systems and participate in corrective and preventive actions (CAPA) and other Quality Management System (QMS) activities.
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Experience leading SAP ME and/or SAP DMC project implementations Functional knowledge and hands-on experience with LIMS (Laboratory information management system), QMS (Quality management system), and MAM (Manufacturing asset management.
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The successful candidate will partner with both internal and external chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges and be skilled in the art of modern organic synthesis, purification, and analytical data interpretation.
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Pay Information $3,099 per week About The Position Weekly Pay Range - $2790 To $3099 Summary : The Echo Tech produces quality images of heart muscle and functions; Sets up ultrasound equipment; records cardiac data and measurements using high frequency sound waves (ultrasound), and other noninvasive echocardiography testing equipment.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application.
$103,500 - $170,800 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Working knowledge of nucleic acids DNA/RNA analytical performance assessment tools: PCR, Cloning/plasmid generation and design, Quality control on DNA/RNA (capillary electrophoresis, UV quantification, Sanger sequencing, NGS.
$51.72 - $57.72 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Oversee all aspects of external (CMDO/CTL) GMP quality control operations including data review, quality event assessment and resolution (laboratory investigation, deviations, impact assessments, CAPAs, change controls.
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Minimum of 5 years of hands-on MDM experience in the areas of MDM Strategy, Architecture, Design, Integration, Data Quality and Data Governance. Collaborate with Data Quality & Data Governance Organization to assist with the monitoring and preservation of the quality of the master data.
Full-timeExpandApply NowActive JobUpdated 6+ months ago
data quality jobs in Burlington, MA
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