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The QA/QC Supervisor is responsible for the implementation of the RES Quality Management System and the execution of the Quality Control Processes and Procedures for the Project Site Construction Team. In conjunction with the HSQE Quality Manager, the QA/QC Supervisor develops and maintains the Construction Quality Plan and the Inspection Test Plan (ITP) throughout the duration of their assigned project; the position is 100% site based.
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Maintain all x-ray equipment, including calibration, QA/QC procedures, and record keeping in accordance with current policy and procedures. Ensure all Radiology workflows are followed and all Radiology reports cross correctly to EMR Follows documentation procedures and completes required documentation related to patient x-ray visit.
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Previous experience as a QA/QC TECH in a bakery warehouse with a firm understanding of allergen handling and GMPs 1+ years related experience, preferred. H&F Bread Company ("H&F")- QA/QC TECHs will be responsible for ensuring all company personnel and visitors are following Good Manufacturing Practices (GMPs), Sanitation Standard Operating Procedures (SSOPs) and food safety preventive control requirements for regulatory compliance.
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Perform QA/QC procedures for the imaging equipment PACS and prepare necessary documentation. Demonstrates the ability to provide accurate and complete documentation of patient procedures with correct entry of charges at the time service is delivered.
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Develop, review, and/or revise QA/QC procedures, work instructions, QMS supporting documentation (technical editing). The Human Performance Quality Assurance Manager will provide quality assurance/quality control (QA/QC) support to the human performance labs in the Biomedical and Environmental Research Department (BERD), Human Health and Performance Contract at Johnson Space Center.
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Assists team leader in ensuring that documentation for all phases conforms to QA/QC and HOK Best Practice Standards. Applies proper QA/QC methods throughout project.
$95,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Charter cross functional tech transfer teams comprising of R&D, QA, QC, Regulatory Affairs, and operations. Responsible for developing biologics process control strategy document, technology transfer change controls, engineering, clinical, and PPQ batch protocols in coordination with R&D and ensuring that the manufacturing batch record meets established conditions as defined in the CMC documentation.
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Manages and completes Compliance Assurance Monitoring system activities including compliance documentation QA/QC, fugitive LDAR, and stack testing; conducts compliance audits and provides other environmental surveillances, manages storage tank roof seal inspections, recordkeeping and reporting.
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Previous experience in managing QA/QC construction materials testing, inspection, and/or geotechnical engineering projects. Our construction services include daily observation / inspection, project documentation, submittal review, design support, shop drawing review, payment application review, payroll review, and oversight for materials testing.
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Proven experience in working with and understanding the various needs of Oklahoma Department of Transportation (ODOT), or Oklahoma Turnpike Authority (OTA), or other transportation entities. In this role, you will oversee the personnel that provide administration, management, inspection, and observation of construction projects for clients like Oklahoma Department of Transportation, Oklahoma Turnpike Authority, and local municipalities.
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Planner must build job plans that clearly show special instructions and required documentation such as MOC information, QA/QC needs, P&ID’s, spec sheets, required skill crafts and duration, specialty tools, equipment and reserve or create purchase orders for necessary components.
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Ensures execution of the QA/QC programs and ISO requirements about all operations and documentation requirements. Coordinate all relevant QC records pertaining to the calibration, validation and maintenance of equipment, and the continuous training of employees and maintain all quality management records for the Microbiology department.
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Establish close out documentation requirements and distribute to site teams Ensure QA/QC is being followed and report any issues/gaps Coordination and management of all Owner-direct vendors working with supply chain and consultants People Management Lead a team of direct and matrix report.
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Follow all QA / QC procedures, protocols, and adhere to laboratory policies and procedures related to accreditation and safety standards. Author detailed forensic laboratory notes and supporting documentation.
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Work with Superintendents to develop the project plans, weekly schedule updates and monitor QA/QC. Review the schedule and weekly narrative to ensure the project is tracking for on-time completion and documentation is in accordance with the MSA / Prime Contract Agreement.
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