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The Systems Engineer I is responsible for assisting in the development and management of requirements and specifications, system integration and testing of electromechanical, fluidic, thermal control, and imaging systems, and formal verification and validation testing.
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Manages, develops and/or oversees the Quality team's responses to all QMS issues to timely close including; non-conformances, performance of Risk Assessments, CAPA investigation and support, design validation, QMS improvements and enhancements, NCR's, compliance with regulations, policies, procedures, external and internal audits, Technical support issues, etc.
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Your Role We are hiring an experienced Validation Engineer to support multiple commissioning, qualification, and validation projects. 5+ years in a equipment commissioning, qualification, and validation engineering role, including proven success developing and executing validation protocols in the pharmaceutical manufacturing industry.
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Be a Technical Leader for the projects across global cross-functional teams (Product / Project Management, SW COE, Electrical Integration, Train Control, Office Systems, Safety, Validation and Applications Engineering) assuring "cradle to grave" success.
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This role will be initially focused on the Software Dev area of CP, developing services around the following 4 themes: Platform Services, Lifecycle, Validation, Data Hub, Global Operational Excellence and will require a close partnership with the Spectre Engineering team as well as all Commerce Platform Pillars.
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As a System Validation Specialist, you have hands on experience with installing, troubleshooting, repairing, calibrating, and inspecting monitoring equipment used in healthcare facilities. The System Validation Specialist will maintain a local stock of necessary parts, ensuring efficient execution of tasks, and will actively engage with customers to provide updates on projects and address service-related issues.
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Trouble shooting PRISM validation errors. SAP Materials Management and Unison PRISM integration would be ideal. Trouble shooting PRISM financial interface errors. Trouble shooting PRISM validation errors.
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We are seeking an Embedded Test Engineer to support the development projects with a leading battery energy storage integrator in the DC Metro Area. You will be responsible for validating the quality and reliability of embedded software products through formal testing and validation processes.
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2-3 years of field service experience with industrial instrumentation and controls validation. Familiarity with programs/software such as Rockwell Factory Talk, Tridium, Schneider Electric, Siemens Apogee, Ignition, Eaton Networks, Field Servers, Jace Controllers, Modbus RTU/TCP, Bacnet, Niagara.
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You have provable hands-on experience with large-scale service APIs, big data, distributed computing and an understanding of things like High Availability, Failover, System testing/validation, Common Vulnerabilities and Exposures.
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Experience in Systems Engineering with an emphasis in requirements development, test planning, test documentation, and systems integration, verification, and validation. Fibertek, Inc. is a leading developer of laser and electro-optic systems for the aerospace community, with key contributions to lasers for atmospheric sensing, laser communications, and lidar sensors for NASA, DoD, and commercial customers.
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The Senior Manager, Valuation & Capital Market Analytics – Model Risk Management (MRM) is responsible for managing the execution and delivery of challenging Model Risk Management related engagements by performing risk management related activities such as designing effective challenge and validation of models, independent review of model documentation and governance, writing high quality model validation reports and will the initial proposal preparation through project completion.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Prior experience developing Cameo model validation scripts. Prior experience developing Cameo model validation scripts. Demonstrated experience with Agile program execution and using agile tools (e.g. Jira and Confluence.
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Generate ideas and design experimental plans for target identification and validation in vitro and in vivo. This candidate will be responsible for developing therapeutic hypotheses via model development, target ID and validation and drug discovery.
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Prepare/review development reports, tech transfer and process validation documents, regulatory submissions. Proficiency in protein purification principles and methods including (but not limited to) different modes of chromatography, viral removal/inactivation steps and filtration.
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validation job in Potomac, MD
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