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Generates required documentation to complete the Device History Record (DHR) Must be able to read and understand: detailed test instructions, assembly instructions, work orders, test results, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assists in creating and updating process and product documentation. Knowledge of LEAN Manufacturing, Six Sigma tools and concepts, Demand Flow Technology (DFT) Experience testing and troubleshooting: laser based optical systems, fluidic systems, digital and analog circuitry.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Must be able to read and understand: detailed aaaaa instructions, assembly instructions, work orders, aaaaa results, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes.
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Ivc.edu. Paper copies are available in the District Human Resources (DHR) office upon request. Documentation according to USCIS I-9 guidelines (i.e. ID card and Social Security card) must be presented at the time of hire.
Part-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Based in San Clemente, CA, you will be responsible for building and preparing components, subassemblies, and top-level assemblies, complete documentation and data input into an MRP system and/or Batch Records (BRs) and Device History Record (DHR.
$31,000 - $40,300Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform DHR Review of manufacturing performed while working on potential improvements to the overall documentation process. Word processing, spreadsheet, Internet, e-mail, manufacturing, statistical and database software such as Minitab or JMP.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Act as liaison to central service agencies for timekeeping responsibilities (e.g., State Controller’s Office, DHR, etc.) Identify and compile requested payroll documentation for audits and submit responses to Payroll Supervisor, Payroll Lead, and Controller.
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Generates required documentation to complete the Device History Record (DHR) Analyzes test results on defective units to determine root cause of failure. Generates required documentation to complete the Device History Record (DHR) Analyzes test results on defective units to determine root cause of failure.
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Perform prompt DHR review in compliance with FDA regulations and Good Documentation practices. Prior experience working in electronic documentation systems preferred but not required.
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Medical device,New product development,Solidworks,Design,Mechanical engineering,R&d,Research & development,Design control,Validation,Design History Record,DHR,Design change. Medical device, New product development, Solidworks, Design, Mechanical engineering, R&d, Research & development, Design control, Validation, Design History Record, DHR, Design change.
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Knowledge and understanding of document control, design transfer, verification, validation, acceptance activity, DMR, DHR and electronic signature requirements to ensure that product, equipment, tools, processes, software, training and documentation meet requirements.
$95,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Processes and archives all documentation into locked filing cabinets, including updating trackers, scanning into electronic document management systems (eDMS), creating labels and filing. Executes Quality Assurance deliverables such as DHR reviews, label reconciliation, and other quality assurance deliverables as required.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Ensure appropriate device history record (DHR) documentation. The position of Manufacturing Line Quality Engineer is within our Infectious Disease. Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life Science or other.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You will also be responsible for preventive maintenance on specific equipment and documentation for department manager review and approval as well as supporting and participating in the maintenance of the clean room and environmental chambers, manufacturing equipment, and keeping the cleanliness of the clean room in accordance with cGMPs/QSR requirements.
TemporaryExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Crate Create engineering standards that will feed into our NPI process to ensure the plant to customer rigging process is consider for proper tooling. Work well in a cross functional team environment (Logistics, Order management team, Service, Engineering and EHS) to identify high risk operations because we have the lack or proper tools for product handling and/or rigging methods.
Full-timeExpandApply NowActive JobUpdated Today
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