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Lead IT Validation Consultant

Amaze Systems Inc

New York, USA

Contract, Third Party

Lead IT Validation Consultant Remote Notes : Prior experience in CROs, clinical research organizations, or pharmaceutical/biotech companies. Knowledge of laboratory processes such as PK, TK, and biomarker studies. Experience with integration of LIMS with other lab or enterprise systems (e.g., CDS, ELN, CTMS).Validation or QA certifications a plus. JD: We are seeking an experienced IT Validation Consultant to lead and support the validation of Laboratory Information Management System (LIMS) used

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

Memory Validation Engineer

Cynet Systems

Austin, Texas, USA

Contract

Job Description: Responsibilities: Execute electrical, functional, & system tests of DDR5 and LPDDR5x memory sub-system test plans as part of a post silicon platform engineering team using hardware and software validation tools, oscilloscopes, and logic analyzers. Develop technical test plans and tools to support platform level silicon bring-up and the validation execution of DDR5 and LPDDR5x memory subsystems. Analyze & debug electrical and functional test data to drive into production SOC a

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

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

SUD Validation Engineer

Thermo Fisher Scientific

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

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

Verification and validation Engineer

Boston Technology Corporation

Santa Barbara, California, USA

Contract

We are looking for a Validation Engineer to designs and develops software test programs for automated and manual testing of Infrared systems. Onsite Engineering verification or validation is required Requires knowledge of Windows as a development and test environment. Linux is a plus Experience writing test code for reuse, executing test cases, and generating reports Experience with PyTest will be very helpful Experience with software version control (SVN, Git), project tracking, and bug-trackin

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

GE EMS Expert / EMS Validation Specialist and RT SCADA

PeakIT

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

Computer System Validation

Smart Source Technologies

Jacksonville, Florida, USA

Contract

Computer System Validation Jacksonville, FL Onsite 12 months contract Pay : $55/hr W2 or $60/hr C2C Job Description:- Working knowledge of FDA and European medical device regulations (QSR and ISO) is required. Working knowledge of software validation requirements for software used in the production of medical devices and software used to support the Quality System is required. Working knowledge of GAMP5 and SDLC is required. Working knowledge of regulations for electronic records, electronic

Hardware Validation Testing Tech

Cloud Destinations LLC

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

Project Manager (Independent Verification and Validation) - Lansing, MI

Digital Technology Solutions

Lansing, Michigan, USA

Contract

DTS is looking for experienced Project Manager (Independent Verification and Validation) for a direct client position in Lansing, MI Top Skills & Years of Experience: 5+ years of IT project management experience, preferably supporting large, complex technology initiatives.5+ years providing Independent Verification and Validation (IV&V) or equivalent quality assurance services.Bachelor's Degree in Information Technology, Business Administration, Project Management, or a related field required.Pr

RT SCADA to EMS - GE EMS Expert / EMS Validation Specialist

Cloudious

US

Contract, Third Party

Job Title: RT SCADA to EMS GE EMS Expert / EMS Validation Specialist Location: Remote Job Type: 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 in elect

PM-Independent Verification and Validation (IV&V)

Resource Consulting Services

Lansing, Michigan, USA

Contract, Third Party

Role: PM-Independent Verification and Validation (IV&V) Duration: 1 year with possible extension. Location: Lansing, MI 48933 Hybrid Local candidates only In-person Interview Client is seeking a seasoned professional with direct experience establishing Independent Verification and Validation (IV&V) services in a complex, enterprise-level environment. This role is not intended for individuals who have performed validation and verification as a secondary responsibility within project management.

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

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

Senior Pharma GxP Project Manager with a strong background in SAP S/4 HANA validation

Pioneer Corporate Services Inc

Foster City, California, USA

Contract, Third Party

Job Title: Senior Pharma GxP Project ManagerLocation: Hybrid Foster City, CA (Locals or nearby states preferred)Duration: 12 Months Job Description:We are seeking a Senior GxP Project Manager with a strong background in SAP S/4 HANA validation and Life Sciences industries. The role demands excellent stakeholder and change management skills, hands-on validation expertise, and solid project leadership. Must-Have Skills: 15 20 years of overall experience 8+ years in Computer System Validation (CSV)

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

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

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