Validation Analyst Jobs in California

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SAP DATA Validation Analyst (Finance, HANA, Power BI)

PY DATA, INC.

•

Remote or Loveland, Colorado, USA

Contract

SAP DATA Validation Analyst (Finance, HANA, Power BI) Loveland, Colorado 80538 12+ months SAP Data Validation Analyst (Finance) - Were seeking an experienced SAP Finance/HANA consultant for a 12+ month contract to resolve critical data validation issues between SAP, HANA, and Power BI. Core Business Problem: Data reconciliation failures between SAP HANA Power BI causing millions in quarterly audit discrepancies with their auditor. Need someone to eliminate the bottleneck where accounting sta
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Posted 26 days ago | Updated 1 day ago

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

•

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 60+ days ago | Updated 1 hour ago

Sr. Analyst, IT Validation Services

Russell, Tobin & Associates

•

Remote or Stamford, Connecticut, USA

Contract

Job Title: Sr. Analyst, IT Validation Services Location: Remote Duration: 12 Months Pay Range: $30/hr-$35/hr on W2 (DOE) Primary Responsibilities Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls: Validation Plans/Summary Reports Risk Assessments User Requirements Specifications Test Plans Test Scripts: IQ, OQ or PQ Assess and implement the most effective validation strategy for each activity. Oversee test execution for c
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Posted 45 days ago | Updated moments ago

Hardware Validation Engineer- Irvine CA

Belcan Services Group, Limited Partnership

•

Irvine, California, USA

Contract

Job Title: Hardware Validation Engineer Location: 14600 Myford Road, Irvine CA 92606 Duration: 12 months Pay Rate: $55/hr. Job Description: Responsibilities: Validation Planning & Criteria Development: Develop and manage comprehensive validation plans for mechatronic systems and sub-systems, ensuring all design and performance requirements are met.Establish testing criteria for accurate and reliable results, including sample size, statistical analysis, and attribute vs. variable testing.Test Pla
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Posted 5 days ago

Hardware Validation Testing Tech

Cloud Destinations LLC

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Santa Clara, California, USA

Contract

Key Responsibilities: Hardware Validation & Testing: Execute test plans for chips, GPUs, and data center hardware to evaluate performance, reliability, and power consumption.Use lab equipment (oscilloscopes, logic analyzers, PCIe analyzers, etc.) to collect and analyze data.Assist in debugging failures, working closely with validation engineers to identify issues and propose solutions.Document test results and report anomalies for further analysis. Software & Automation Testing: Write and execut
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Posted 16 days ago

QC Validation Support Specialist Carlsbad, CA Onsite

MARVEL INFOTECH Inc

•

Carlsbad, California, USA

Contract, Third Party

QC Validation Support Specialist Contract Location: 100% Onsite Carlsbad, CA Local to California only Must have: Pharma/Biotech/Medical Device, IQ/OQ/PQ, GxP / cGMP, Commissioning and Qualification Background: The Radioligand Therapy (RLT), Carlsbad site is installing new instruments and software in the laboratory that will require validation work for the new QC lab. As a part of the onboarding of new QC equipment and instruments for the project, multiple QC instruments, and QC support equipme
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Posted 3 days ago | Updated 3 days ago

FPGA Validation Engineer (Vivado)

Mirafra Inc

•

San Jose, California, USA

Full-time

Develop and execute post silicon Validation and Characterization for clocking circuits on in some of the industry s largest and most complex SOCs (using Xilinx s FPGA design tools such as Vivado/ISE).Hands-on experience with lab equipment such as oscilloscopes, logic analyzers,Thermosteamer, Clock generators and other equipment.Expert knowledge and hands-on experience of the entire backend and adjacent flows, including synthesis, Floor-planning P&R, clocking, timing closure, power, and IO plann
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Posted 14 days ago | Updated 1 day ago

Validation Engineer

Source Code Technologies LLC

•

Sunnyvale, California, USA

Contract

Role name: Validation Engineer Branch | City | Location: Sunnyvale/ Santa Clara, CA Duration: 6 Months Keywords: Key Words to search in Resume Computer System Validation, 21 CFR Part 11, GxP, FDA, 21 CFR Part 11, ISO 13485, IEC 62304 Role Description: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development.Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product sof
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Posted 4 days ago

GE EMS Expert / EMS Validation Specialist and RT SCADA

PeakIT

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Remote

Contract

Job Title: RT SCADA to EMS GE EMS Expert / EMS Validation Specialist Location: Remote Job Type: 12 Months Contract Role Overview: We are seeking a highly skilled RT SCADA to EMS Expert with deep experience in GE EMS platforms, real-time data integration, and EMS validation processes. This role will be instrumental in supporting the deployment, integration, and validation of SCADA/EMS systems to ensure secure, stable, and efficient grid operations. Ideal candidates will have a strong background i
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Posted 23 hours ago

IQ/OQ/PQ Validation Engineer with Medical (W2 Only)

Sovereign Technologies

•

Irvine, California, USA

Full-time

Title: Sr. Validation engineer with Medical Device Candidates Location: Onsite in Irvine, CA Duration: 2+ years 1) Word copy of resume 2) 2-3 professional references THIS IS NOT A SOFTWARE POSITION Looking for hands on IQ/OQ/PQ Validation in Medical Device Candidates MUST HAVE Bachelor of Science in Engineering or a related subject with 4+ years of experience in validation GMPs.Good understanding of engineering and machine tool fundamentals.Written and owned the validation processSME on IQ/OQ/PQ
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Posted 3 days ago

Silicon Validation Engineer

Sivaltech

•

San Jose, California, USA

Full-time, Third Party

Job Summary: We're looking for silicon validation engineers to drive pre-silicon and post-silicon validation of SerDes and High-Speed interfaces for automotive products. You'll develop test plans, test cases, and automation scripts using Python, and collaborate with design, DV, and firmware teams. Responsibilities: - Develop validation test plans and methodologies - Create test cases and automation scripts using Python - Develop low-level drivers for Windows and Linux OS - Collaborate with tea
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Posted 10 days ago

Need - Computer Software Validation (CSV) Engineer

ASCII Group LLC

•

Santa Clara, California, USA

Contract, Third Party

Hi, The following requirement is open with our client. Title : Computer Software Validation (CSV) Engineer Location : Santa Clara, CA (ONSITE) Duration : 12+ Months Relevant Experience (in Yrs.) : 8+ Job Description: Minimum of 4-5 years of experience in software quality assurance or software validation, preferably within the medical device industry.Strong understanding of quality standards and regulatory requirements (e.g., FDA 21 c, ISO 13485, IEC 62304).Experience with non-product software v
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Posted 5 days ago

System Validation Engineer

Katalyst Healthcares and Lifesciences

•

Santa Clara, California, USA

Full-time

Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards. Ensure computerized systems are appropriately validated Assessment of applicabi
Posted 1 day ago | Updated 1 hour ago

Sensing HW Validation Engineer (Test Engineer III)

WinMax Systems Corporation

•

Cupertino, California, USA

Contract

Job Title: Sensing HW Validation Engineer (Test Engineer ) - 36081285 Job Duration: 12+ Months Job Location: Cupertino, CA - Fully Onsite Job Summary: The Sensing HW team develops groundbreaking sensors that are central to a variety of Client's platforms, including iPhones, iPads, Audio, Macs, the Home ecosystem, and accessories. You will play a key role in developing, characterizing, and validating sensor systems used in these platforms. The ideal candidate will have expertise in touch sensin
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Posted 53 days ago | Updated 2 days ago

Automotive Validation Technician - Environmental Testing

BayOne Solutions

•

Torrance, California, USA

Contract

Must Have Ability to work hands onAble to read electrical schematicsElectrical testing/troubleshooting experienceExperience with High Voltage (800 1000V)Experience with Microsoft OfficeHarness Fabrication Nice To Have Build Technician ExperienceMachine shop toolsSolderingTechnical degree in electronics Responsibilities: Set up and run development and validation tests (thermal, vibration, humidity, corrosion, electrical performance) on High Voltage Power ElectronicDocument test results and prov
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Posted 60+ days ago | Updated 24 days ago

Computer System Validation (CSV) Engineer

Katalyst Healthcares and Lifesciences

•

Remote or Massachusetts, USA

Full-time

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. uthor and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's degree
Posted 2 days ago | Updated 1 hour ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

•

Remote or New Jersey, USA

Full-time

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles. Compliance Analysis, Validation Planning, Risk Assessments Test planning and strategy creation and execution of test protocols, scripts and reports. V
Posted 60+ days ago | Updated 1 hour ago

System Validation Engineer

SUPERMICRO COMPUTER INC

•

San Jose, California, USA

Full-time

Job Req ID: 26864 About Supermicro: Supermicro is a Top Tier provider of advanced server, storage, and networking solutions for Data Center, Cloud Computing, Enterprise IT, Hadoop/ Big Data, Hyperscale, HPC and IoT/Embedded customers worldwide. We are the #5 fastest growing company among the Silicon Valley Top 50 technology firms. Our unprecedented global expansion has provided us with the opportunity to offer a large number of new positions to the technology community. We seek talented, pass
Posted 28 days ago | Updated 1 hour ago

Sr. Validation Engineer (CSV)

Katalyst Healthcares and Lifesciences

•

California, USA

Full-time

Responsibilities: Create and execute Computer System Validation (CSV) deliverables (Validation Plans, Protocols, Reports, Trace Matrices, SOPs). Collaborate with Business Users, System Owners, IT teams, and Analysts to define validation requirements. Provide leadership and training in validation activities. Generate IQ/OQ/PQ protocols using Good Documentation Practices (GDP). Ensure compliance with quality system elements for computer systems/software testing. Perform gap assessments and remedia
Posted 60+ days ago | Updated 1 hour ago

Engineer III, Validation

Thermo Fisher Scientific

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Remote or Fair Lawn, New Jersey, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you're part of Thermo Fisher Scientific, you'll do meaningful work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the
Posted 53 days ago | Updated 1 hour ago