principal validation engineer Jobs

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Product Validation Engineer

Aditi Consulting

•

Coffeyville, Kansas, USA

Contract

Payrate: $48.00 - $50.68/hr. Responsibilities: Plans, coordinates, perform product design, testing and/or analysis work for a complete project of moderate scope or for a significant portion or a sub-system of a major and diverse project. Operates in a team environment, providing input to design solutions and participating in design reviews. May assign, coordinate and review portions of the work to support personnel. Decisions are made within established guidelines and may be reviewed by supervi
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Posted 2 days ago | Updated 8 hours ago

Electrical Power Electronics Test & Validation Engineer

Tranzeal, Inc.

•

Newark, California, USA

Contract

Role: Electrical Power Electronics Test & Validation Engineer Location: Newark, CA (Onsite) Top 3 Hard Skills Required Strong understanding of power electronics topologies and control.Minimum 5 years experience with Strong hands-on and trouble-shooting skills in testing and verification of power electronics systems, including the use of lab equipment (battery simulators, power supplies, E-loads, scope, etc.).Minimum 5 years experience with Strong technical writing and communication skills, wi
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Posted 2 days ago

SUD Validation Engineer

Thermo Fisher Scientific

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Logan, Utah, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing so
Posted 26 days ago | Updated 1 hour ago

System Validation Engineer

Katalyst Healthcares and Lifesciences

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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 9 days ago | Updated 1 hour ago

Silicon Validation Engineer

Sivaltech

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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 18 days ago

Sr. Validation Engineer (CSV)

Katalyst Healthcares and Lifesciences

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Muskegon, Michigan, USA

Full-time

Roles & Responsibilities: The Validation Specialist carries out quality control checks on engineering project work under the supervision of the Validation Lead, Automation Lead and Project Manager. Perform initial CSV at client site for systems including DeltaV, Historian, MES, ABB as well as other DCS and OT systems. They will review and approve risk assessment link to CSV of systems. Collaborate with the other departments, within their respective areas of responsibility for Change Managemen
Posted 7 days ago | Updated 1 hour ago

Principal Engineer, Hardware & Silicon Validation

Marvell Semiconductor Inc.

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Westborough, Massachusetts, USA

Full-time

About Marvell Marvell's semiconductor solutions are the essential building blocks of the data infrastructure that connects our world. Across enterprise, cloud and AI, automotive, and carrier architectures, our innovative technology is enabling new possibilities. At Marvell, you can affect the arc of individual lives, lift the trajectory of entire industries, and fuel the transformative potential of tomorrow. For those looking to make their mark on purposeful and enduring innovation, above and be
Posted 57 days ago | Updated 1 hour ago

Computer Systems Validation Engineer

Katalyst Healthcares and Lifesciences

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Bethlehem, Pennsylvania, USA

Full-time

Job Description: We're seeking an experienced Computer Systems Validation (CSV) professional to join our team and lead end-to-end validation activities supporting laboratory system upgrades and data integrity initiatives. This role is ideal for someone with a strong background in regulated environments and hands-on experience with modern lab software and instrumentation. This is a short-term contract assignment running through September and requires individuals to work onsite. Responsibilities
Posted 1 day ago | Updated 1 hour ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

Santa Clara, California, USA

Full-time

Roles & Responsibilities: Software quality assurance or software validation. Preferably within the medical device industry. Strong knowledge of FDA 21 CFR Part 820, ISO 13485, IEC 62304. Experience in non-product software validation. Includes tools for development, testing, maintenance. Deep understanding of quality standards and regulatory requirements: FDA 21 CFR Part 820. ISO 13485. IEC 62304. Software quality assurance. Software validation. Non-product software tools (for testing
Posted 1 hour ago

Principal Process Controls & Validation Engineer

Regeneron Pharmaceutical

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Rensselaer, New York, USA

Full-time

Regeneron is currently looking for a Principal/ Staff Process Controls & Validation Engineer for the Labeled Drug Product fill/finish manufacturing processes. This is Monday-Friday, 8am-4:30pm schedule. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering, and mathematical needs from the laboratory to the manufacturing floor. This role provides technical support to manufacturing, quality and CMC Regulatory for manufacturing processes f
Posted 60+ days ago | Updated 1 hour ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Irvine, California, USA

Full-time

Job Description: The Senior Validation Engineer will serve as a subject matter expert in validation, leading critical projects in support of GMP-compliant manufacturing and product development. This role involves strategic planning, execution, and continuous improvement of validation processes across multiple sites, while supporting audits, risk assessments, and global quality initiatives. Responsibilities: Interpret and implement validation requirements based on FDA regulations, corporate stan
Posted 7 days ago | Updated 1 hour ago

Senior Validation Engineer

Cloud Destinations LLC

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Santa Clara, California, USA

Contract

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 designing, executing, and analyzing validation tests, as well as hands-on experience with Python scripting for test automationand software testing methodologies. The idea
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Posted 60+ days ago | Updated 2 days ago

Computer System Validation (CSV) Engineer

Katalyst Healthcares and Lifesciences

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Remote or Massachusetts, USA

Full-time

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. Author 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
Posted 17 days ago | Updated 1 hour ago

Associate Manager, Data Validation Engineer

Takeda pharmaceutical

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Boston, Massachusetts, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by
Posted 12 days ago | Updated 1 hour ago

Validation Engineer

Salas O'Brien Engineers Incorporated

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Houston, Texas, USA

Full-time

At Salas O'Brien we tell our clients that we're engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That's why we're committed to living our values every day: inspiring, achieving, and connecting as shared owners of our success with a focus on a sustainable future. Building for the long-term means that all of our team members can expect to work on amazing projects with a people-first approach to problem solving. It also means
Posted 8 days ago | Updated 1 hour ago

Validation Engineer

Katalyst Healthcares and Lifesciences

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Summit, New Jersey, USA

Full-time

Responsibilities: Maintains all qualified and validated equipment and systems in compliance with policies, guidelines and procedures. Develops protocols, and associated reports while adhering to a change management process. Supports the execution of equipment qualifications and validation protocols. Supervises vendors for qualification functions. Supports equipment qualification and systems validation activities. Configures and documents the configuration of computerized systems. Develops
Posted 16 days ago | Updated 1 hour ago

System Validation Engineer

SUPERMICRO COMPUTER INC

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San Jose, California, USA

Full-time

Job Req ID: 26975 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 22 days ago | Updated 1 hour ago

Sr. Validation & Verification Engineer

ConsultNet, LLC

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Salt Lake City, Utah, USA

Full-time

Sr. Verification & Validation Engineer (onsite) Salt Lake City, UT Contract to hire Pay: $50-$65/hr Job Description: We are looking for a Senior Verification and Validation (V&V) Engineer to lead the development and execution of our testing strategy across hardware, embedded software, and clinical software systems. In our fast-paced startup environment, this role will be critical in planning, executing, and documenting V&V activities to ensure the safety, effectiveness, and regulatory compliance
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Posted 1 day ago | Updated 1 hour ago

Senior Engineer Computerized System Validation

Takeda pharmaceutical

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Social Circle, Georgia, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the Role: The Computerized Systems Validation Engineering, is responsible for leading, managing, and performing engineering op
Posted 28 days ago | Updated 1 hour ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

•

San Juan, San Juan, Puerto Rico

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.
Posted 60+ days ago | Updated 1 hour ago