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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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Employ CBA data visualization and editing tools to aid in the efficiency of gap analysis in CBA development, generating Joint Capabilities Integration and Development Systems (JCIDS) products, and provide a persistent data model that will reduce the need to re-create data across multiple program documents, and will feed requirements documentation, allocation, and tracking tools such as Dynamic Object-Oriented Requirements System (DOORS.
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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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Utilizing knowledge and understanding of cGMP (Current Good Manufacturing Practices), ISO standards, and the company's Quality Management System, the Facilities Engineer will oversee the coordination, compliance, and documentation requirements for all facilities projects.
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In this role as a General Neurologist, you will serve the culturally diverse community in the suburbs of the city of Lowell, MA. Working with a multidisciplinary team, offering continuity of care for patients all within one practice, you will have support with flexible scheduling allowing for documentation time within your workday.
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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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RMF, NIST, and NISPOM requirements, configurations, settings, and documentation. Ensure that authorization/re-authorization support documentation is developed and maintained in conformance with applicable standards.
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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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Ability to author site work plans, reports, and proposals for complex scopes of work. Remediation Expertise: Evaluate subsurface characteristics for soil, soil vapor, and groundwater remediation projects, and apply remedial systems and solutions.
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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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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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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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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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author documentation jobs in North Billerica, MA
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