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Author technical documentation for AP1000 primary components (e.g. steam generator, pressurizer, PRHR, core makeup tank and accumulator) and operating plant replacement steam generator design documentation, including but not limited to, design specifications, design reports, E&DCRs, and various calculation notes.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Author, Review, Approve and Execute CSV life cycle documentation. Hands on experience in Implementation & Validation of various computerized systems like PCS (DeltaV) / BAS (Rockwell) / MES (Syncade) and Pi Historian / SCADA / PLC.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Author and review GMP documentation related to process development (protocols, Design of Experiments (DOEs), SOPs, Change Controls, ). AnazaoHealth compounds preparations for Age Management, Weight Management, IV Therapy, Sexual Health, Vitamin Injections, Hormone Replacement, Hair Care Solutions, Aesthetics and more.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Gather database design and configuration specifications from the Sponsor· Review DB designs to ensure consistency with protocol requirements· Review custom data validation rules and checks for completeness and logic· Performs UAT testing of database design and design updates, ensures all test documentation is complete prior to DB release· Author and update CDM control documents, including Data Management Plan, SAE reconciliation, Laboratory / PK reconciliation plans, etc.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The CRM/ Back End Web Developer will perform web development using open-source web programming languages (e.g., Ruby, Python) and frameworks (e.g., Django, Rails); develop and consume web-based, RESTful APIs; work in team environments that use various methodologies (e.g., Scrum, Lean); author developer-friendly documentation (e.g., API documentation, deployment operations); test-driven development techniques; use version control systems (e.g., Git and GitHub.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Solid Dose Process Development Scientist will report to the Facilities and Engineering Manager in support of process development, scale up, and process validation. AnazaoHealth is a specialty compounding pharmacy focusing on Wellness, Pain Management and Nuclear Medicine.
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This is your opportunity to act as a technical support resource specialist in the field of wetland ecology and mitigation, biology, regulatory compliance, NEPA documentation, and other federal, state, and local permitting, such as critical areas permitting in Washington State.
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Extensive experience in BICR reader selection and performance monitoring and improvement •Deep understanding of collection and QA of imaging and related non-imaging data from sites to Imaging Vendor to Sponsor •Clear comprehension of computation and programming of BICR output (e.g., ORR, PFS, DoR) Familiar with good documentation practices and record retention processes, particularly those used in Biostatistics and Data Management groups.
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Professional-level English, spoken and written and direct experience designing, creating and reviewing technical documentation both architecture, operational and self help guides for IT Departments and end users.
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In addition, the Software Test Engineer will work with System Engineers, Developers and other Testers to accurately author the test based documentation required for the project. Author and execute manual and automated test cases to ensure product requirements are met.
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Author/support the program documentation of the HFE processes and products in a format consistent with US Military Data Item Descriptions (e.g. Human Engineering Program Plan, Human Engineering Design Approach Document – Operator, Human Engineering Design Approach Document – Maintainer, Human Engineering Test Plan, Human Engineering Test Report, etc.
$107,300 - $160,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Author, and/or review of GLP/GMP documentation in accordance with GDP requirements, including protocols, reports and raw data. Documentation is detailed, timely and in compliance with Process Development requirements.
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Author and maintain tools, techniques, and practices for assuring the testing of the product. Write testing documentation and help finalize all system and software documentation CDRLs for the program.
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Ability to author technical reports and comfort utilizing electronic documentation workflows for review, approval, and archival. Support regulatory inspections and filings as an author and reviewer.
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This role will support equipment development and maintenance activities facility operations, process development activities, support compliance investigations/change management, and author GMP documentation in any of our enabling facilities.
Full-timeExpandApply NowActive JobUpdated 2 days ago
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