Data validation Jobs

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Validation Engineer with Ciena Routing & Switching - Middletown, NJ (Remote is also fine)-Telecom Industry Prefer

GLOBAL IT CON LLC

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Remote or Middletown Township, New Jersey, USA

Contract

Job Title: Validation Engineer Job Location: Middletown, NJ (Remote is also fine) Job Duration:12 months Job Description: This position allows you to assist customers in optimally crafting, deploying, operating, and continuously improving cost-effective solutions based on a Service-Aware Operating System (SAOS) based Routing & Switching portfolio (RSP) and its associated network management platform. This is an on-customer premise technical role with a focus on facilitating customers to understan
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Posted 15 days ago | Updated 15 hours ago

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

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Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana
Posted 7 hours ago

Validation Engineer

Indotronix International Corp

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Durham, North Carolina, USA

Full-time

Role: Validation Engineer Location: Durham, NC Pay Rate: $40/Hr on W2 Duration:6+ Months Scope of Position: Reporting directly to the Quality Engineering Supervisor, this position involves product team support for the manufacturing operations, provides quality guidance, product resolution decisions, and statistical problem-solving techniques to manufacturing operations and projects teams for new product introduction, process improvements, continuous improvements, and validation activities. This
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Posted 19 days ago

System Calibration & Validation Technician(Hardware/Software)(Oscilloscope,Calibration)

Tellus Solutions

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Roseville, California, USA

Contract

Job Description: Description: The Americas region of client is looking for a systems' support technician. The successful candidate will be part of a small team in the regional quality and engineering organization, supporting calibration systems used in the Americas' calibration labs. Responsibilities:Ensure the high uptime of calibration controllers and the SW running on them for the service delivery teams.Manage the computer refresh program of the Americas region consisting of installation and
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Posted 5 days ago

Sr. Software Validation Engineer

Talascend

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Newark, California, USA

Contract

Talascend is currently seeking an experienced Sr. Software Validation Engineer for a contract-to-direct career opportunity with our client on-site in Newark, CA. Candidates must be eligible to work for any employer without sponsorship now, or in the future. W-2 only. Relocation at the candidate s expense will be considered. This role does not support remote or hybrid work. Overview The engineer will work collaboratively with a team responsible for cybersecurity of embedded systems (ECUs); per
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Posted 7 hours ago

Validation - Project Manager

Futran Solutions

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Seattle, Washington, USA

Full-time

Job Description: Location: Seattle-Dexter, WA*Hybrid Top Skills: - Experience in the Biotech/Cell Therapy industry Preferred - PMP Experience Preferred - Experience with Smartsheets, Tableau, and MS Projects - Strong organizational skills, ability to multi-task and work in a dynamic, fast paced environment. The Project Manager is closely partnered with the GMS&T Leader to enable effective execution of strategy and plans. The scope of responsibilities of the Project Manager fall into 4 general c
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Posted 36 days ago | Updated 16 days ago

Computer Systems Validation Engineer

Katalyst Healthcares and Lifesciences

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Rocky Mount, North Carolina, USA

Full-time

Responsibilities: Resolution of fundamental Computer System Validation compliance issues on assigned projects Writing, reviewing, and executing computer validation documentation. Perform computer system validation activities related to process control systems of pharmaceutical water for injection system, water pretreatment system, water stills and high-quality steam generation systems. Validation of computerized systems, in accordance with GAMP5 and V-Model (USR, Function Specification, IQ/OQ/Pr
Posted 7 hours ago

PSV Engineer (Post-Silicon Validation)

Avance Consulting

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Sunnyvale, California, USA

Full-time

8+ years of experience in AMS, specifically in post silicon validationExperienced in AMS Test developmentExperience in PMIC, Data converters testingWell-versed in lab automation using Python, LabVIEWExperienced in debugging, troubleshooting using lab equipment s (Scope, analyzer, SMU, power supplies etc)Well-versed in communication and has leadership skills
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Posted 11 hours ago

Hardware Validation Engineer

BayOne Solutions

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Plymouth, Michigan, USA

Contract

Note: - This role is 100% onsite with time at supplier locations throughout Southeast Michigan (about 4 days per week in Troy and 1 day in Livonia MI). Job Overview: We are seeking a skilled Validation Engineer to develop and manage validation plans for vehicle hardware subsystems in vehicle programs. The ideal candidate will play a crucial role in ensuring that all systems meet performance targets through rigorous validation processes. This position requires close collaboration with external te
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Posted 20 days ago | Updated 2 days ago

Senior Software QA Engineer

PsiQuantum

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Remote or Palo Alto, California, USA

Full-time

Quantum computing holds the promise of humanity's mastery over the natural world, but only if we can build a real quantum computer. PsiQuantum is on a mission to build the first real, useful quantum computers, capable of delivering the world-changing applications that the technology has long promised. We know that means we will need to build a system with roughly 1 million qubits that supports fault tolerant error correction within a scalable architecture, and a data center footprint. By harnes
Posted 60+ days ago | Updated 8 hours ago

Computer System Validation Specialist

SGS Consulting

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Remote

Contract

Job Title: Computer System Validation (CSV) Specialist Duration: 08 Months + (Possible Extension) Location: Wilmington, DE 19803 (Remote) Schedule: M-F: 08 AM 05 PM Kindly Do not apply if you are not or Permanent Resident of USA. Qualifications: The official position title is Computer System Validation (CSV) specialist to support the Newark manufacturing facility with validation of new and existing computerized systems.This role will primarily support the Newark manufacturing facility but may r
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Posted 21 days ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Maple Grove, Minnesota, USA

Full-time

Responsibilities: Define the development of comprehensive specifications (hardware and/or software) for equipment/software from basic functionality to complex systems such as PLC's, Visual Basic applications, databases, SCADA applications, and systems with FDA defined electronic records and electronic signatures. Provide project estimates independently. Review estimates for Engineer I's. Submit specification, protocol and report for approvals and documentation control vi Change Request. Develop
Posted 7 hours ago

Sr. CSV Validation Engineer

Katalyst Healthcares and Lifesciences

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New Brunswick, New Jersey, USA

Full-time

Responsibilities: Review computerized systems validation documents such as: Requirements Specification, Design Specification, CSV Risk Assessment, Test Plans, Test Summary Reports, Data Migration Plan, Pre/Post Executed Test Scripts, Traceability Matrix. Release to Production Statements Direct and review testing Provide guidance on quality issues that affect the integrity of the data, or the system Obtain and respond to QA review. Participate in establishing standard quality and validation pract
Posted 7 hours ago

Sr. CSV Validation Engineer

Katalyst Healthcares and Lifesciences

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Lawrence Township, New Jersey, USA

Full-time

Roles & Responsibilities: 8-10+ Years of Overall IT Experience Review computerized systems validation documents such as: Requirements Specification, Design Specification, CSV Risk Assessment, Test Plans, Test Summary Reports, Data Migration Plan, Pre/Post Executed Test Scripts, Traceability Matrix. Release to Production Statements Direct and review testing Provide guidance on quality issues that affect the integrity of the data, or the system Obtain and respond to QA review. Participate in
Posted 7 hours ago

CSV Validation Engineer

Katalyst Healthcares and Lifesciences

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Austin, Texas, USA

Full-time

Roles and Responsibilities: Strong writing, grammar, and editing abilities to create clear and concise documentation. bility to adapt writing style to various audiences (e.g., end users, technical teams, or regulatory bodies). Document Design and Formattingo Proficiency with documentation tools. Knowledge of design principles to create well-structured documents (manuals, user guides, SOPs, etc.). Version Controlo Familiarity with tools like Git, SVN, or SharePoint to manage document revisions a
Posted 7 hours ago

Senior Validation Engineer

Katalyst Healthcares and Lifesciences

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Marlborough, Massachusetts, USA

Full-time

Responsibilities: Derive test requirements from the design specifications, define test plan and methodology, estimate effort and resources plan to cover design verification and validation campaign. Establish acceptance criteria, sampling, assess through modeling or qualitative/quantitative testing, evaluate the performance according to URS, SRS (design inputs and outputs). Write test protocol, setup design of experiments, execute tests, analyse results and document reports for design verificati
Posted 7 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Raynham, Massachusetts, USA

Full-time

Responsibilities: Ask candidates if they have validated equipment and what type of equipment they have validated. Mechanical/manufacturing experience. Writing and executing validation protocols. CSV is nice to have, but if the candidate has done that exclusively it will not work. Requirements: A minimum of a Bachelor's degree in Engineering is required. Minimum of 1-3 years' experience in medical device manufacturing, Bio/pharma is also good Develop and implement processes to support the
Posted 7 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Hartford, Connecticut, USA

Full-time

Responsibilities: Functional requirement specification, function risk assessment, installation qualification, operational. Qualification, performance qualification, traceability matrix, project release notes, system certification summary). Execute validation activities in computerized system and ensure 21 CFR part 11 compliance. Knowledge in GAMP. Preparing risk assessment for functional requirements and providing testing strategy, implementing technical & procedural controls as part of mitigat
Posted 7 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Framingham, Massachusetts, USA

Full-time

Responsibilities: Execute validation activities in computerized system and ensure 21 CFR part 11 compliance. Knowledge in GAMP. Preparing trace matrix to ensure requirements are tested to meet the software intended use. Preparing risk assessment for functional requirements and providing testing. strategy, implementing technical & procedural controls as part of mitigation. Preparing SOP/Work instruction for equipment and software-based systems. Requirements: 6 to 8 years of Non-Product Software
Posted 7 hours ago

Senior Validation Engineer

Katalyst Healthcares and Lifesciences

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Pomona, California, USA

Full-time

Responsibilities and requirements: 6 to 8 years of Non-Product Software Validation engineer with Manufacturing background (Medical devices or Diagnostics). Non-Product software validation for Manufacturing Equipment's as per Regulatory standards (FDA, ISO requirements). Prepare, review functional requirements, design and testing documents. Prepare, review of SLC deliverables (Validation plan, change requests, User requirements specification, Functional requirement specification, function risk a
Posted 7 hours ago