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Provide expertise in the preparation and production of contract documentation including proposal technical writing, project schedules and fee estimate support. Have the ability to advance detailed design documentation for construction solicitation under supervision.
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Conduct thorough reviews of vendor documentation and perform QA/QC checks on supplied equipment and contractor engineering. Proficiency in industrial process control instrumentation and analyzers, (SIS), and industrial electrical systems (120V - 6900V, motors, substations, switchgear.
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The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service providers.
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Contributes to firm's TKM by developing white papers and technical design documentation of new or special case designs, studies, etc. Under direct supervision, creates basic to moderate complexity engineering designs involving site layout development, site grading and drainage, hydraulics and hydrology calculations, water distribution systems, collection systems, storage tanks and impoundments, foundation designs, stormwater infrastructure and treatment, and occasionally single-story structures.
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Ability to utilize process safety documentation such as P&IDs, HAZOPs, Process Flow Diagrams. Ownership of Safety Critical documentation such as Process and Instrumentation Diagrams" (P&ID's), Electrical Classification, equipment files processes to ensure accuracy.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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A dynamic company in Suffolk is on the hunt for a Quality Engineer to be the linchpin for their quality assurance efforts. Documentation: Create and review cGMP documentation, ensuring everything is up to snuff.
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We are seeking a skilled Validation Engineer with experience in GxP compliance and expertise in 21 CFR Part regulations. Proven experience as a Validation Engineer in the life sciences industry.
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Documentation tools experience like Visio, MS Word, Confluence, Excel, Splunk etc. 3+ years of Red Hat Linux or UNIX support experience. 3+ years of Grid computing platform experience (IBM Spectrum Symphony or Tibco Grid Server.
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Completes all calibration, qualification and validation documentation with accuracy, completeness and compliance to Celgene standards. Completes all calibration, qualification and validation documentation with accuracy, completeness and compliance to Celgene standards.
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This role may support facility operations, process development activities, support compliance investigations/change management, author GMP documentation and manage/lead engineers in any of our enabling facilities.
$107,700 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Oversee an Assistant Resident Engineer and field staff to ensure that they are properly carrying out their functions of ensuring proper installation and advancement of construction and they are filing the proper documentation.
$75 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Manage vendors performing calibration and preventative maintenance work in the Flex STERILE Center – request quotes, issue PO’s, review JSA’s, ensure vendor qualifications, schedule work escort vendors, and review and file completed documentation.
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Network Engineer with Automation/JIRA, Confluence exp. Project Management Tools: Familiarity with Agile project management tools like JIRA and Confluence for tracking tasks and documentation.
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We are looking for an experienced Automation & Controls Engineer/Manager to join a Global Pharmaceutical company. Maintain GMP and work with the regulatory team to ensure all documentation adheres to compliance standards and company standards.
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