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Documentation required to support end of line validation, shipping, operations, maintenance, commissioning, and validation. Completion of the validation, assessments, and documentation to ensure the product is fully Safety compliant with regional requirements.
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The Commissioning Intern is responsible for supporting automation projects and will be capable of component selection, device troubleshooting, HMI development, PLC programming and debugging, Software debugging, onsite system checkout and startup, and validation of System Throughputs and Efficiencies.
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This role will be responsible for developing lab automation data integration strategies and architectures for the global quality laboratory automation projects, including information system (ELN, LIMs) integration with vendor-independent laboratory work cells and computer system validation (CSV.
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PACIV, an international control systems integration and regulatory compliance engineering firm servicing Bio-Pharmaceutical, Medical Device, F&B, and Water/Wastewater clients, is looking for a full-time Validation Engineer (Level I) team member for our USA office (Indianapolis.
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Job Title : Functional Safety Engineer. Focus on all the Safety aspects of the Hydrogen Generation and Purification System. Job Title : Functional Safety Engineer. Geo Blue PPO and HSA plan. MetLife Dental and Vision plan.
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Perform the mechanical and thermal test, characterization, and validation of power electronics designs. The systems business unit is currently looking for a dynamic, results driven individual to join as a Sr. Engineer, Power Electronics Mechanical Design.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Secondary Loop Process Control Engineer provides engineering solutions to the business, utilizes project management skills and first principles in delivery of these solutions, provides off-hours automation control system support as needed, and can recommend new control strategies for the various chemical processes utilized in pharmaceutical manufacturing operations.
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A System Integration Engineer in the Global Quality Laboratory is an automation position responsible for evaluating technologies to modernize and improve analytical analyses for testing in a manufacturing environment.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The Process Engineer (MS&T Engineer) is responsible for providing technical support for cGMP production runs, tech transfer activities, process engineering, process validation, process monitoring, and biopharmaceutical processes in the cGMP manufacturing facility.
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Continually develop technical aptitude of PF's core capabilities including but not limited to: Project Management Cell and Gene Therapy Capital Projects Facility Builds Tech Transfers Validation Life Cycle Commissioning and Qualification Quality, Regulatory, and Compliance Engineering Automation and Serialization Reliability, Maintenance, and Asset Management.
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Support test and validation to ensure products meet design specifications, including use of precision metrology equipment (optical comparator, non-contact camera and laser systems, coordinate measurement machines, micrometers, etc.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ten (10) or more year’s minimum experience in GMP or regulated operations as validation engineer, process engineer, project engineer, or similar capacity. Associated tasks include equipment specification and procurement, process development, drawing development, protocol development, validation input, and execution.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Technologies used in this position include the full scope of Material Handling with conveyors ranging from simple gravity conveyor up to cutting edge shoe sorters with servo driven diverts, robotics, Automated Storage and Retrieval Systems from a variety of vendors, and complex add on such as automated carton erection or print and applies.
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The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.
$87,152 - $94,600 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Perform data analysis and validation to ensure data quality and integrity. Strong proficiency in Java programming language for data engineering tasks. Create and maintain documentation for data engineering processes and systems.
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validation engineer jobs in Indianapolis, IN
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