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Job Description PharmaLex is one of the largest worldwide providers of consulting services in the following focus areas: Quality Management & Compliance; Development Consulting & Scientific Affairs; Regulatory Affairs; and Pharmacovigilance, Epidemiology and Risk Management.
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Assists in the development and maintenance of a detailed schedule of QA/Reg milestones and deliverables; to include internal audits, quality improvement projects, Trial Master File (TMF) reconciliations, etc.
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Entrada is seeking a Director, GCP/GLP Quality to manage GCP and GLP quality assurance activities. Works across all levels in the organization to deliver GCP/GLP Quality compliance.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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Full ownership and accountability for all Quality Controls Assurance programs, activities and reviews, including claims reviews; call center and digital communications reviews; Medicare Risk Adjustment, HCC, clinical and coding reviews; DRG and medical records reviews; technology/systems and coding upgrade and implementation reviews (e.g. final user acceptance testing, etc.
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Experience in a biotechnology or pharmaceutical company, with 10+ years of direct involvement in analytical development and/or quality control of protein biologics. This individual will be responsible for overseeing key deliverables in analytical development such as method development, assay qualification, release/stability, in-process assays, in-use stability methods, quality control, and quality assurance aspects of Spyre’s pre-clinical & clinical biologics product candidates while partnering with other Tech Ops development groups and quality assurance.
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Maintain robust GMP quality systems, including documentation, change control, deviations, CAPA, and quality events. A minimum of 7 years of experience in GMP quality assurance within the biotech or pharmaceutical industry, with direct experience in auditing and the manufacture of monoclonal antibodies or biologics.
$170,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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S/he would also provides support for the NACA’s Mortgage Operations in providing quality control and auditing for the various NACA departments. The QA Analyst is responsible for the overall evaluation of NACA systems and software to ensure they are free of defects and meet the quality standards of the organization.
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As a Quality Control Manager- Rail, you will play a critical role in the overall leadership and successful and timely delivery of complex multimillion-dollar fast-track, complex heavy-civil, highway and bridge projects from pre-construction stage through project execution and completion.
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The Associate Director, Biomarker Operational Quality will provide biomarker quality leadership and oversight across GxPs-related to research and development, implementation into clinical trials and potential commercialization of clinical biomarkers into IVDs. This leader will collaborate with business partners and GCP Operational Quality to drive quality outcomes and operational excellence.
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Supplier Quality Engineer - Interconnect Commodity - Remote. We are looking for a Supplier Quality Engineer to implement tools and processes to ensure suppliers improve on current products with robust plans and deliver first time quality to BAE program customers.
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CDM Smith is looking for a Water Resources Engineer to support our Ecosystem Restoration and Water Quality Practice. Water Resources Engineer - Water Quality. Water quality permitting support, including anti-degradation studies, National Pollutant Discharge Elimination System (NPDES) permit applications and appeals, and permitting strategy.
Full-timeExpandApply NowActive JobUpdated 11 days 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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This role will offer the opportunity to learn ETQ & Windchill applications to facilitate updates of documentation, develop and enhance KPIs to monitor Quality team processes, and participate in continuous improvement exercises to mature Quality team processes.
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This role will support the Quality Department at both our Andover HIP and Andover Product Fabrication sites, in all areas as listed in essential job functions, working closely with Quality Manager.
ExpandApply NowActive JobUpdated 4 days ago
quality job Title: manager Company: Experian in Boston, MA
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