WiFi Validation Engineer - Onsite - Menlo Park, CA Jobs

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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 10 days ago | Updated moments ago

Vitros Validation Scientist (ONSITE)(No C2C/H1B)

NetSource, Inc.

•

Rochester, New York, USA

Contract

Please note that this is a 12+ contract position ONSITE in Rochester, NY No C2C or H1 visas. Just available in W2 basis QualificationsMinimum BS degree in a scientific field (Chemistry, Biology, Biotechnology, or Chemical Engineering preferred); MS or PhD preferred 5 7 years of experience working in a regulated environment (FDA, ISO, USDA, etc.) Experience with VITROS MicroSlide technology required Experience with QO Change Control systems (or equivalent) required Experience with data analysis i
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Posted 3 days ago | Updated 3 hours 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 4 days ago

Sr. Validation Engineer (CSV)

Katalyst Healthcares and Lifesciences

•

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 8 days ago | Updated moments ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

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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

Platform Validation Engineer

Horizontal Talent

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US

Contract

We are seeking a talented Platform Validation Engineer to join our dynamic team. This role offers a unique opportunity to work on cutting-edge technology in a hybrid work environment, contributing to the future of computing. ResponsibilitiesConduct hardware platform testing and pre/post-silicon validations to ensure optimal performance.Develop and implement system-level tests for SoC and peripherals, reporting progress and issues effectively.Engage in debugging and troubleshooting, particularly
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Posted 5 days ago | Updated 4 days 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 60+ days ago | Updated 12 days 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 2 days 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 day ago | Updated moments 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 60+ days ago | Updated 1 hour ago

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
Posted 60+ days ago | Updated moments ago

Validation Lead

TechDigital Corporation

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King of Prussia, Pennsylvania, USA

Third Party, Contract

Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP applications and is able to perform document/process Compliance Analysis Adept with Agile and Waterf
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Posted 26 days ago

Systems Engineer (Sys Integr, Ver & Validation)

Boeing Company

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Everett, Washington, USA

Full-time

Systems Engineer (Sys Integr, Ver & Validation) Company: The Boeing Company Refer to "Supplemental Information" for further clarification on the use of this job family. In locations where SPEEA representation applies, this job family will be covered by the terms of the collective bargaining agreement. Applicable and appropriate educational/certification credentials from an accredited institution and/or equivalent experience is required. Language Requirements: Not Applicable Education: Bachel
Posted 3 days ago | Updated 1 hour 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. 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 11 days ago | Updated 1 hour ago

Validation Support Engineer

Katalyst Healthcares and Lifesciences

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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
Posted 59 days ago | Updated moments ago

Lead Hardware 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. This role requires deep expertise in designing, executing, and analyzing validation tests, as well as hands-on experience with Python scripting for test automation and software testing methodologies. The ideal candidate will play a critical role in ensuring the reliability, performance, and functionality of cutting-edge hardwa
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Posted 4 days ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

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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

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 8 days ago | Updated moments 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 29 days ago | Updated 1 hour ago

Space Vehicle Verification and Validation Lead - Blue Ring

Blue Origin, LLC

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Seattle, Washington, USA

Full-time

Application close date: Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We're working to develop reusable, safe, and low-cost space vehicles and systems within a culture of safety, collaboration, and inclusion. Join our team of problem solvers as we add new chapters to the history of spaceflight! The role is part of the In-Space Systems business unit, which is
Posted 13 days ago | Updated 9 hours ago