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Operational experience with a Threat Emulation or Breach & Attack Simulation platform such as Verodin, Mandiant Security Validation, or AttackIQ. Experience working within a Security Operations Center (SOC), red team, purple team, or blue team.
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Expertise or interest in antibody-drug conjugates, immune-oncology, CAR-T cells, and T-Cell engagersExpertise in the design, optimization, validation and analysis of immunohistochemistry and multiplex immunofluorescence assays, and image analysis.
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Participating in activities to the delivery acoustic STDA capabilities which include one or more of the following: Requirements Definition, Funding Requirements; Analysis and Engineering; System Analysis and Design; System Integration and Test; Validation and Verification; System and Operational Performance Analysis; and Decision Analysis and Resolution.
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The Antenna Engineer will work on one project close to launching into the market (in the testing and validation stage) and two new projects that have completed conception(the full implementation stage.
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A good understanding of FDA and ICH guidelines and practical knowledge with assay validation and cGMP will be advantageous. This role is pivotal in the development, qualification, and validation of molecular separation assays for testing vaccine products.
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Provide engineering studies, technical engineering support, training and leadership to manufacturing, QA, validation, Quality Control, Validation, Facilities, and Metrology for continuous process improvement, troubleshooting, change control and deviation resolution.
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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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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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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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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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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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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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validation job in Gaithersburg, MD
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