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The position requires the ability to work through each step of an analysis, which may include external visual photo-documentation, electrical test, non-destructive troubleshooting, environmental testing, x-ray evaluation, destructive testing, decapsulation, cross-sections, internal visual photo-documentation, scanning electron microscope (SEM) evaluation, and writing a detailed final report.
$77,000 - $163,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform other administrative documentation and record keeping, such as accountability and statistical reports, billing forms, student intern evaluations, performance evaluations, etc. Ensure clinical documentation is complete and according to departmental standards.
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Transfer studies to and completes proper documentation of these studies the McKesson Cardiac CPACS. Qualifications: Education: Graduate of an approved program in Echocardiography Experience: Pediatric experience preferred.
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Primary Sterile Processing responsibilities include receiving instrumentation, sorting and decontamination of procedural items and instrumentation; inspection and assembly of minor instrument groups and instrument trays; identification of respective sterilization method and cycle selection, accurate documentation for all sterile processes; and accurate inventory assignment relating to the case building process.
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This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client’s facility.
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Maintain daily and monthly progress notes, shift checklists, and other program documentation according to DDS, DMH, and all applicable regulatory standards. Provide services to individuals according to, DDS, DMH, MassHealth, HUD, DPH, CARF, all applicable regulatory standards, and Bridgewell policies and procedures.
$15 - $18.85 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Extensive knowledge in various business functions, enterprise, semiconductor manufacturing, engineering design and processesCommunication and collaboration with extended global teams, both within IT and outside IT.Additional Skills, Knowledge and AbilitiesStrong presentation and technical documentation skillsStrong organizational skills and the ability to work and lead a team to aggressive schedules.
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Participate in the technical writing, review of documentation & regulatory submissions and facilitate the Tech Transfer process. The role is well-integrated into the rest of the MSAT Microbial Team. This role will collaborate with other MSAT scientists to setup bioreactors and execute well-designed experiments, including but not limited to basic analytics, data acquisition and documentation of work.
$25 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Follows CMOP policies regarding documentation and reports to meet VA and TJC policy. Provides full checking, labeling, and quality assurance within the guidance (written VHA handbooks, written CMOP policies, and training that will be provided by the CMOP) of the Department of Veterans Affairs regarding pharmaceutical medications.
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Execute material transactions in company ERP system and use carriers' computer systems to generate shipping labels, packing slip import/export documentation and manage document filing systems. Execute material transactions in company ERP system and use carriers' computer systems to generate shipping labels, packing slip import/export documentation and manage document filing systems.
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Support pharmaceutical manufacturing plant, equipment, and utilities, and maintain compliance with all state and federal guidelines with emphasis on current Good Manufacturing Practices (cGMP) and Good Documentation Practices (cGDP) requirements.
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Experience working with electronic document systems (CMMS work orders, LMS, Track Wise, Master Control) or similar systems. Interact with and direct vendors for manufacturing improvement and plant maintenance (i.e. HVAC, Clean Utilities, trades) primary support for Security/System Monitoring/Fire System, janitorial services, and waste water certifications.
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Demonstrated experience conducting NEPA / CEQA / other analysis and preparation of associated documentation. Comply with regulatory requirements pertaining to the data integrity, documentation, procedures, training, monitoring systems, reporting, and record compliance and retention.
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Assist Patient Care Manager in clinician documentation review/audits to ensure complete, appropriate, and accurate submission of all documentation by field staff. a part of LHC Group family of providers – the preferred post-acute care partner for hospitals, physicians, and families nationwide.
Starting at $36 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage the procurement and build of proof of design Circuit Card Assemblies (CCA) and Modules which includes reviewing the Bills of Material (BOM) to source parts, communicating with suppliers to obtain quotes and provide International Traffic in Arms Regulations (ITAR) controlled documentation.
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author documentation jobs in Tewksbury, MA
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