Validation Analyst jobs

Cupertino, California

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30+d ago

A globally leading technology company is looking for a Hardware Validation Engineering Program Manager to join its world-class hardware team. In this role, you will drive end-to-end validation efforts, ensuring that new hardware and system features are thoroughly tested and meet performance and reliability standards before reaching customers. You will collaborate with cross-functional engineering teams to assess risk, execute validation plans, and communicate key issues, risks, and mitigation st

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Contract

$70 - $85

Validation Engineer

Buffalo Grove, Illinois

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Today

Job Description: Strong knowledge of ERP systems. (implementations/validation). Expert writing test scripts, test functionality, data flow, documentation. CSV-Computer systems validation. Requirement management exp. (supporting planning for requirements, integrating requirements and the organization for working with them). Has worked in the manufacturing/med device space.

Full-time

Validation Engineer

Chillicothe, Illinois

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Today

Aspire IT Solutions is in a need of - Role: Validation Engineer Location: Chillicothe, IL (Onsite) Duration: 12 months contract Job Description: Seeking a detail-oriented Validation Engineer to ensure software systems, applications, and embedded solutions meet all functional, performance, and compliance requirements. The ideal candidate will have strong experience in testing, automation, and hardware/software integration. Required Skills & Experience: 5+ years of experience in validatio

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Contract, Third Party

Validation Engineer - GxP Systems

San Francisco, California

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Today

Responsibilities: Lead and manage CSV (Computer System Validation) for GxP systems across Quality, Manufacturing, Clinical, and Business areas. Develop and maintain validation procedures, templates, and master validation plans. Prepare and review validation documentation (plans, protocols, reports). Ensure compliance with GAMP 5, 21 CFR Part 11, and ISO 13485. Collaborate with cross-functional teams (IT, QA, Engineering, Manufacturing, Clinical). Support change control, audits, CAPA, and documen

Full-time

validation Engineer (Medical devisse)

Hillsboro, Oregon

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Today

The Opportunity: In this exciting role, you will apply knowledge of qualification and validation principles, manufacturing processes, quality systems, engineering design fundamentals, health authority expectations and industry standards to provide quality oversight for the site qualification/validation program. You will perform quality oversight of qualification and validation activities associated with equipment, facility and utility systems, GMP computerized systems, drug product manufacturing

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Contract

$50 - $60

Hardware Validation Engineer

Spokane, Washington

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9d ago

Position Summary: You will be responsible for the creation and execution of electrical test plans. This includes writing test plans based on product documentation and functional specifications, using software test tools and test automation, performing tests, documenting test results, and validating product defects. This position supports the validation of next-generation Networking products integrating Intel Xeon CPUs, AMD Versal and Altera Agilex FPGAs, Marvell Ethernet switches, and 400Gb opti

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Contract

Depends on Experience

Manufacturing Process Validation

Plano, Texas

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29d ago

Minimum experience of 10 years in Medical devices - Manufacturing Engineering. Good Experience working on Process Validations (IQ, OQ, PQ) Experience developing manufacturing processes and technologies, which includes process characterization Experience working on PFMEAs Experience performing Data analysis (Minitab) Evaluate process and design alternatives based on Design for Manufacturability principles. Ability to work within a team and as an individual contributor in a fast-paced, changing en

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Third Party, Contract

$40 - $45

Validation Engineer

Raritan, New Jersey

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Today

Job Description: We are seeking an experienced Validation Engineer with strong expertise in SAP and OpenText systems, combined with technical writing/documentation skills. This role is critical in ensuring compliance, validation, and accurate documentation of enterprise applications, particularly in regulated environments (GxP/21 CFR Part 11). Responsibilities: Perform Computer System Validation (CSV) activities for SAP and OpenText systems. Develop and execute validation protocols (IQ, OQ,

Full-time

IT CSV & CQV Validation Lead

Boston, Massachusetts

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Today

Responsibilities: Documentation & Deliverables: Develop and author comprehensive validation and quality documentation, including protocols, reports, risk assessments, SOPs, and other project-related materials. Ensure all documentation complies with applicable regulatory standards such as FDA, EMA, GxP, and other relevant guidelines. Review and approve validation documents to confirm alignment with both project objectives and regulatory requirements. Project Management: Lead and oversee multiple

Full-time

OTA Validation/Test Automation Engineer

Sunrise, Florida

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3d ago

Onsite Role OTA Validation/Test Automation Engineer Sunrise, FL 12+ Months Contract Position Type- W2 Only Exp Level- 7 Years Req Skills- OTA SW Upgrade / Downgrade, Over-the-air (OTA), ECU Flashing, performing software updates via OTA, 3G/4G TCUs, NAVI, HMI Modules, Python, C#, ECU Test, HIL Validation Platforms like DSPACE, Vehicle Automation Testing, Issue management, Defect Management, Version Management tools like JIRA, Github, SVN,, UDS Protocol, Validating Diag over CAN, DOIP, CAN, LIN P

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Contract

Depends on Experience

Staff Validation Engineer (West Hills, CA)

Los Angeles, California

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Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardotoxic materials Job Description When you're part of Thermo Fisher Scientific, you'll do exciting work and be part of a team that values performance, quality, and innovation. As part of a su

Full-time

USD 103,100.00 - 154,700.00 per year

Computer Systems Quality Assurance (CSQA) with Validation (CSV)

Indianapolis, Indiana

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30+d ago

Job Title: Computer Systems Quality Assurance (CSQA) with Validation (CSV) Location: Indianapolis, IN (Onsite) Duration: 12+ Months Job Description: Please not that 1 F2F round is mandatory. Mandatory skills: IT CSV Validation of IT systems IT QA / QA eCompliance Manager Experience with Veeva Quality Docs, ServiceNow, JIRA and HP ALM Pharma industry experience is mandatory Medical device experience is good to have This Computer Systems Quality Assurance role will be responsible for supporting

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Full-time, Contract, Third Party

$DOE

Validation Engineer II

La Verne, California

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Today

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical ro

Full-time

USD 99,705.00 - 129,030.00 per year

Engineer Product II - Product Verification & Validation

Fargo, North Dakota

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Today

Job Title: Engineer Product II - Product Verification & Validation Location: Fargo, ND Duration: 12 Months + Possibility to extend Shift: 1st shift Pay Range: $50/hr - $53/hr W2 E-machine Module Team Overview Sourcing & Design Collaboration Client does not manufacture their own electronic motors, instead sourcing them from a global supply base (e.g., Dana, Molly). Motors are not purchased off-the-shelf; Deere selects the right motor for the application and collaborates with suppliers and i

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Third Party, Contract

$ $50/hr - $53/hr W2

Computer System Validation Engineer

New Jersey

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Today

Roles & Responsibilities: Bachelor's degree in computer science, Engineering, Life Sciences, or related field. 3-7 years of experience in CSV within pharmaceutical, biotech, or medical device industries. Strong knowledge of GAMP 5, FDA 21 CFR Part 11, Annex 11, and related guidelines. Experience with ERP, LIMS, MES, or other GxP systems. Extensive Experience in HPALM with Manual testing. Deep knowledge in Defect Management Life cycle. Proficient in writing validation protocols, reports, and SOPs

Full-time

Propulsion Verification and Validation

Everett, Washington

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Today

Role :- Verification & Validation Engineer with Propulsion Location :- Everett, WA- Onsite Type :- Full Time Job Description: Verification & Validation Engineer with Propulsion Completion of Safety requirements and JIRA actions Propulsion Verification exp DRO ( Design Requirement Objective)/SRO (System Requirement Objective) verification GTRs: validation, deallocation and deferral activity Revision of requirements process co-ordination sheet Validation activity for DRO allocation from outsid

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Full-time, Contract

BASED ON EXPERIENCE

Computer System Validation - CSV Engineer

Remote or New Jersey

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Today

Roles & Responsibilities: Minimum 8+ years of relevant experience; can work independently and guide/mentor Junior resources. Experience in the Pharmaceutical, biotechnology, or medical device industry with System Development Lifecyle in Computer System Validation Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Knowledge of FDA guidance's and industry standards (i.e., GAMP) Experience in writing and executing documen

Full-time

Post Silicon Validation Engineer - Onsite

Austin, Texas

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4d ago

Title: Post Silicon Validation Engineer Onsite Mandatory skills: PCIe, CXL, USB, SATA,C, C++, Python, Perl,server OS, Windows Server, Ubuntu, RedHat,SoC, SoC validation, SoC issues, SoC debug,Datacenter Server, BIOS, system firmware, CPU part socketing,PC architecture, Server products, test execution, test equipment, test progress,oscilloscope, protocol analyzer, lab, Card, riser board insertion, minor board rework,document failure analysis, troubleshooting failures, platform setup, platform con

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Contract

Depends on Experience

Validation Engineer

Hillsboro, Oregon

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Today

Responsibilities: Be responsible for the review of system documentation according to the Roche CSV SOPs and regulatory guidance. Develop plans and reports such as validation plans/reports, test plans/reports (and other deliverables). Update existing validation deliverables and procedures in collaboration with the system owners. pply ALCOA+ principles to validation deliverables and quality management system records. Support in deviation investigations to identify root causes and define corre

Full-time

Senior Silicon Validation & Prototyping Engineer

Morrisville, North Carolina

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Today

Our client, a leader in advanced silicon engineering, is seeking a Senior Silicon Validation & Prototyping Engineer to join their team. As a Senior Silicon Validation & Prototyping Engineer, you will be part of the engineering department supporting cutting-edge hardware platforms. The ideal candidate will have strong problem-solving skills, excellent communication abilities, and a collaborative mindset which will align successfully in the organization. Job Title: Senior Silicon Validation & Pro

Full-time

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Validation Analyst jobs