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As the QC Manager your responsibilities include overall management of the Contractor's Quality Control (CQC) with the authority to act in all CQC matters for the Contractor, Herman Construction.
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Implement, develop, and sustain the DAP Quality Management System which includes: Safety, Documentation and Change Control, Supplier Control, Measurement Systems Analysis and Calibration/Validation, Product Conformance, Process Control and Capability, Complaint Investigation/Root Cause and Corrective Action Implementation, Continuous Improvement, Training, and Semi-Annual Auditing.
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For three decades, our best-value companies have provided federal and commercial clients with superior quality and cost-effective, innovative, and sustainable solutions for general construction, restoration services, civil works, fuels systems, environmental services, professional services, and facility support services.
$105,000 - $125,000 depends on experienceExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Establish, Maintain and Improve GxP Quality System including, but not limited to: Deviations, CAPA, Change Control, Risk Management, Inspection Readiness, Product Complaints, Recall/Mock Recall, Internal Audit/Self-Inspection, Supplier Quality Management (incl AVL, QAG and Audit Management), Auditor Qualification, OOS/OOT, CSV, Data Integrity, Training and Document Control.
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Provide comprehensive support for post-market surveillance activities, encompassing complaint investigations, Operations change control/risk assessments, document control, Quality Systems enhancements, Regulatory & certification audit preparedness, and internal audits.
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This role is responsible for directing, monitoring, and managing the quality systems (including Management of Change, Document Control, Label Control, Complaint/Nonconformance, Internal Audits), and associated trainings.
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Demonstrated knowledge of the Deviation (ETS), Change Control (ETS), ValGenesis, ERP (SAP) and Laboratory Information Management (LIMS) systems. Primary responsibilities include: assistance with area batch record reviews and applicable product release, participation in the Change Management, Investigation, and CAPA systems, maintaining the site’s compliance with Zoetis Quality standards, review and approval of action items, performing internal audits and support and quality oversight of.
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Experience performing commissioning, qualification & change control activities related to BMS including but not limited to HVAC, chiller plants, domestic and process water systems, building automation systems, etc.
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The Physical Security Specialist assists in administering and overseeing physical security programs including facility security risk assessments, access control, intrusion alarm systems and CCTV systems, and assists in providing security-related training in a manner consistent with SHI policies, procedures, quality standards and customer needs.
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Protection and control relay engineer will have the opportunity to design and perform relay setting of substation and transmission projects for electric utilities and developers at voltages from 12kV up to 500kV. This is an exciting and growing field in the power systems industry and allows candidates to get exposure to how the power generation such as that of renewable energy ties into the electric system.
$82,400 - $123,600 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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And familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation. Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems such as continuous fill lines (washer, tunnel, isolator, cappers and lyophilization), filling, lyophilization, inspection, as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.
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And familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and. Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems such as cell culture reactors, centrifugation, chromatography, tangential flow filtration, single use systems as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.
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Performs technical tasks in support of all Traction Power equipment, or parts procurements, including specification development, prototyping, design review, first article inspections, systems integration, quality assurance and quality control, quality inspections, safety certification, testing, post-delivery acceptance, reliability test, and warranty support.
$104,299 - $156,448 a yearExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.
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Associate's Degree in business administration, public administration, or closely related field and three years of experience in performing records and document management functions (cataloging and filing) including experience with hard copy and electronic document management systems, records retention, off-site storage and archival processes, configuration management, change control, or quality assurance experience; OR an equivalent combination of education and experience.
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