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Responsible for all aspects of product design including - systems architecture, electrical engineering design, component selection, embedded systems / microprocessor based design and programing, requirements documentation, design verification, design validation, regulatory compliance, test plan creation, test tools and test scripts development, DFM/DFT, design reviews, and DFMEA. Lead projects ranging from short-term technology investigations to full-scale product development.
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During dynamic validations: contributing to validation of the maintenance documentation, maintainability demonstrations, testability (troubleshooting methods), and maintenance execution (preventive and corrective.
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Support Quality Assurance (QA) and Validation departments by drafting design documents and assisting in protocol creation and implementation. Produce documentation to support projects, including project scopes, conceptual design presentations, capital requests, specifications, piping and instrumentation diagrams, process flow diagrams, schedules, requests for quotations, project expenditures, project procedures, correspondences, start-up procedures, and cost estimates.
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Documentation of MES configuration and validation of EBRs. Lead in the design, development, documentation, and implementation of Manufacturing Execution Systems (MES) Understanding of Life Sciences validation processes.
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Their combined job during validation is to fulfill one of the Test & Validation team needs, execute maintenance (corrective and planned), reporting technical anomalies, and developing maintenance execution for fleet service.
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Validation Engineer - I (Assistant). Collaborate with metrology and validation staff across multiple testing labs and sites for system relocations and lab optimization activities.
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Review, and archive instrument/equipment documentation such as master equipment lists, user access reviews, Instrument Installation & operational qualification documentation, and calibration documentation.
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Job Title: CQV Validation Engineer. Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader.
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You will be responsible for analog, mixed signal, and high-speed digital circuit design and simulation, schematic capture, printed circuit board layout, component selection, prototype bring-up, design validation and design documentation.
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Create and maintain documentation as required (e.g. data models, data lineage, metadata, data dictionary, information supply chain) Assist the Risk organization with model validation where needed.
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Job Description: Validation Engineer III. Hands on experience in Implementation & Validation of various computerized systems like PCS (DeltaV) / BAS (Rockwell) / MES (Syncade) and Pi Historian / SCADA / PLC.
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Be responsible for deliverables such as instrument/equipment indexes, instrument datasheets, PLC/DCS card-edge drawings, instrument loop sheets, electrical conduit/cable schedules and riser drawings, control panel design and specification, network drawings, and validation documentation (IQ/OQ.
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Experience in the areas of Design Documentation (URS, FRS, CS, DS, and other engineering specifications) and Validation (OQ, CSV, etc.) Draft and implement Quality System documentation designed to establish good validation practices within the organization.
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Good understanding of cGMPs and good documentation practices in order to prepare system life cycle technical documents such as URS, FRS,VMP, protocol generation and execution to support FAT, SAT, commissioning, qualification (IQ, OQ), SOPs, Validation (PQ, DS, CV, PV), FMEA and Validation Master Plan.
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Overview: Our client is looking for a Validation Staff Engineer located in Middletown, VA. Their customers globally rely on their extensive range of products and services from life-saving medicines to lab essentials to next-generation instruments.
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validation engineer documentation jobs in Jersey City, NJ
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