Validation Engineer II Jobs

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PSV Engineer (Post-Silicon Validation)

Avance Consulting

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

IT Software Validation Engineer

Flextronics

Libertyville, Illinois, USA

Full-time

Job Posting Start Date 05-13-2025 Job Posting End Date 07-14-2025 Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraord

Lead/Senior Validation Engineer

ApTask

Santa Clara, California, USA

Contract

Job Title: Finished Rack Team Lead / Senior Validation Engineer Location: Santa Clara, CA (100% onsite) Duration: 6 months+ Long term opportunity Rate: $55-65/hr on W2 Job Summary: We are looking for a highly skilled Senior Validation Engineer to lead the testing and validation of semiconductor components, data center hardware, and GPUs. Must have strong experience in System Level Validation, which includes rack level systems as well as tray level systems. This role requires deep expertise in de

we have a position for Validation Engineer at Middletown, CT(Onsite)

Dizer Corp

Middletown, Connecticut, USA

Contract

Hi Pals, we have a position for Validation Engineer at Middletown, CT(Onsite) Job Description: Engineer Test and Validation Engineer. Duration:9 Months+ Loc: Middletown, CT(Onsite). In this role, you will be working alongside OEM customer teams performing engineering validation tasks supporting aircraft engine development, testing and certification. Responsibilities Coordinate engine test and/or assembly/tear-down actions between the technicians and IPT/Engineering groups. Communicate technical

Validation Support Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Job Description: We are seeking an experienced Validation Support Engineer to lead validation activities for Beckhoff Twin CAT PLC-controlled systems in a 24/7 GMP-regulated manufacturing environment. The role focuses on ensuring compliance with FDA regulations (21 CFR Part 11, 210, 211, 820), GAMP5 methodologies, and internal quality standards. Responsibilities: Develop/update Validation Plans (VP) and Master Validation Plans (MVP). Lead GxP risk assessments for system changes. Author and

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

GLOBAL IT CON LLC

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

Hardware Validation Engineer

BayOne Solutions

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

CSV Validation Engineer

Katalyst Healthcares and Lifesciences

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

Sr. Validation Engineer (CSV)

Katalyst Healthcares and Lifesciences

California, USA

Full-time

Responsibilities: Creates Computer System Validation (CSV) deliverables (Validation Plan, Requirements Specifications, Protocols, Summary Reports, Trace Matrices, SOPs, Risk assessments). Collaborates with Business Users, System Owner, Global IT teams and Business Analysts to define validation requirements and plans. Providing leadership, oversight, and training related to validation activities to multi-functional teams. Generate and execute validation protocols (IQ/OQ/PQ) using Good Documentati

Validation Engineer

AdientOne LLC

California, USA

Contract

Role: Validation Engineer Location: Santa clara USA 95054| Onsite Duration: 6+ months contract Job Description: In this role, this engineer will be part of a highly technical team that develops test plans, completes functional & electrical validation, & debugs issues for memory controller, NOC & other silicon interface features. Executes electrical & functional test plans for client processors using hardware & software validation tools, oscilloscopes, & logic analyzers. Debug of electrical &

Validation Engineer

Katalyst Healthcares and Lifesciences

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

Validation Engineer

Katalyst Healthcares and Lifesciences

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

Validation Engineer

Katalyst Healthcares and Lifesciences

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

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

Validation Engineer 2

Merck KgaA

Jaffrey, New Hampshire, USA

Full-time

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious mind

Senior Validation Engineer Hardware & Software

Stellent IT LLC

Santa Clara, California, USA

Third Party, Contract

Job Title:- Senior Validation Engineer Hardware & Software Location:- Santa Clara, California(Onsite) Duration:- long term Contract Are you passionate about pushing the limits of semiconductor technology, data center hardware, and GPUs? We're looking for a Senior Validation Engineer to lead critical validation and testing efforts that ensure our cutting-edge solutions deliver on performance, reliability, and functionality. Responsibilities: Develop and execute validation test plans for advance

Validation Support Engineer

Katalyst Healthcares and Lifesciences

Johns Creek, Georgia, USA

Full-time

Roles & Responsibilities: Validation Planning: Develop/update Master Validation Plans (MVP) and individual Validation Plans (VP) for system changes. Required: Proven expertise in CSV (Computer System Validation) methodologies (e.g., GAMP5), FDA regulations (21 CFR Part 11, 210, 211, 820 as applicable), and validation of automated manufacturing/control systems. Experience validating PLC-based systems (Beckhoff Twin CAT experience is a significant plus). Responsibilities: Perform tasks under S

Validation Engineer

Katalyst Healthcares and Lifesciences

Schaumburg, Illinois, USA

Full-time

Responsibilities: Strong understanding of regulations and guidance related to Computer System Validation principles and Quality Management Systems (21CFR Part 11, GAMP- 5, EU Annex 11 and other relevant regulations). Bachelor's degree or equivalent experience in computer science, information technology, or a related field. High degree of proficiency in Microsoft Office Suite and Smartsheet. Detail-oriented with a strong analytical mindset and problem-solving capabilities. Excellent project

Engineer III, Validation

Thermo Fisher Scientific

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

System Validation Engineer

SUPERMICRO COMPUTER INC

San Jose, California, USA

Full-time

Job Req ID: 26644 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