Validation Engineer III Jobs

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Validation Engineer III

Katalyst Healthcares and Lifesciences

•

Mounds View, Minnesota, USA

Full-time

Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Perform, oversee, and guide supplier process validations (IQ/OQ/PQ) for sterile barrier packaging material manufacturing processes. Ensure supplier process validation requirements (CTQs, drawings, specifications, risk levels, and protocols) are communicated, understood, and executed. Collaborate with suppliers to review and approve validation documentation, including prot
Posted 60+ days ago | Updated 7 hours ago

Validation Engineer III

Katalyst Healthcares and Lifesciences

•

Plainsboro Township, New Jersey, USA

Full-time

Job Description: Qualified candidates must be experienced in one or more of the following areas of validation: Equipment Qualification Process Qualification The candidate must utilize problem solving techniques to resolve issues and conflict in order to meet the high level goals set forth by the organization. The candidate must be well organized and technically sound in understanding scientific rationale and justifying criterion from a quantitative standpoint. The candidate must be familiar with
Posted 60+ days ago | Updated 7 hours 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 2 days ago

Sr. Validation engineer with IQ/OQ/PQ Validation in Medical Device in Irvine, CA on W2 basis

Sovereign Technologies

•

Irvine, California, USA

Contract

Duration:2+ years Title: Sr. Validation engineer onsite in Irvine, CA 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/PQFDA Audit experience and ability to be apa
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Posted 22 hours ago | Updated 22 hours 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 50 days ago | Updated 7 hours ago

Engineer III, Validation

Thermo Fisher Scientific

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Remote or Waltham, Massachusetts, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description COMPANY: Thermo Fisher Scientific Inc. LOCATION: 168 Third Avenue, Waltham, MA 02451 TITLE: Engineer , Validation HOURS: Monday to Friday, 8:00 am to 5:00 pm DUTIES: Perform technical diagnosis of operational problems, repairs, and calibrations on a wide range of laboratory equipment to ensure that the equipment is operating to the customer's complete satisfaction and manufacture specifications; Perform techn
Posted 17 days ago | Updated 7 hours ago

Engineer III, Test & Validation

Landis Gyr

•

Lafayette, Indiana, USA

Full-time

At Landis+Gyr, we don't just manage energy-we lead the transformation toward a smarter and more sustainable energy future. With a net revenue of USD 1.73 billion in FY 2024, and a presence in over 30 countries across five continents, Landis+Gyr empowers utilities and consumers to optimize energy usage through advanced metering, grid-edge intelligence, and powerful data analytics. Today, our global team of about 6,300 professionals is shaping the digital energy era-developing innovative technol
Posted 32 days ago | Updated 7 hours ago

Sr. Cleaning Validation Engineer

VetForce Solutions

•

Seattle, Washington, USA

Contract

Sr. Cleaning Validation Engineer Onsite in Seattle, WA 6 month contract to start with likely extensions Musts- 8+ years of experience in cleaning validation within GMP/CDMO environments Strong knowledge of cleaning processes, facility/utilities validation, and regulatory requirements Experience with computer system validation (CSV) preferred Demonstrated ability to write, review, and execute validation documentation
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Posted 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 2 days 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 22 hours 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 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 12 days ago | Updated 1 hour ago

Validation Engineer - Onsite

VIVA USA INC

•

Austin, Texas, USA

Contract

Title: Validation Engineer - Onsite Mandatory skills: Notebook PC Platform Validation, post Silicon validation, LLM, Process Optimization, Process Improvement, .NET, C#, Python, PERL, Bash, Ruby, GITHUB, Virtual Machine, Windows, Linux OS, applications, operating system, regression, processors, hard drives, network cards, memory, Memory, PC Buses, PCIe, USB, SATA, Ethernet, Processor, Chipset, PC Hardware, PC configuration, system validation, tool development, lab, hardware issues, safety tool,
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Posted 18 hours ago

Medical Equipment Engineer I (verification/Validation)

Estuate Inc.

•

Pleasanton, California, USA

Contract, Third Party

Job Summary After introduction to work processes, begins to organize, conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding.Assumes responsibility for the accuracy, quality, and timeliness of experimental results.Summarizes experimental results, and reviews conclusions with supervisors/project leader.Communicates results of experiments. Keeps supervisor/project leader informed of project status, particularly of sign
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Posted 5 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 8 days ago

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
Posted 16 days ago | Updated 7 hours ago

Software Validation Engineer - R&D - Machines

Pro Talent Crafter

•

Johns Creek, Georgia, USA

Contract, Third Party

Role: Software Validation Engineer - R&D - Machines Location: Johns Creek, GA Job Description: Execute validation plans and protocols for R&D projects affecting facilities, equipment, processes, cleaning, and software systems.Perform qualification of equipment such as ovens, sterilizers, HPLC/UPLC systems, molding machines, refrigerators, and freezers.Conduct temperature mapping and environmental monitoring of critical systems.Lead cleaning validation and utility qualification efforts.Write and
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Posted 27 days ago

WiFi/CPE Validation Engineer (Octoscope/Veriwave)

Yoh - A Day & Zimmerman Company

•

Sunnyvale, California, USA

Full-time

WiFi/CPE Validation Engineer Looking for a WiFi Validation Engineer to handle performance testing for routers and extenders. This person must have experience with Octoscope and/or Veriwave - RF Chambers, and be able to write TR-069/TR-181 related scripts. (Octoscope is for OTA testing and Veriwave is for conductive testing). Required: Previous experience with WiFi performance testing is a must have. Octoscope and/or Veriwave is a must have. Octoscope is for OTA testing and Veriwave is for conduc
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Posted 26 days ago | Updated moments ago

Power Electronics Test & Validation Engineer

Advantage Technical

•

Newark, California, USA

Full-time

Position: Power Electronics Test & Validation Engineer Location: Onsite. Newark, CA. Are you an experienced Engineer that's passionate about innovation, sustainability, and cutting-edge technology? If so, consider working for one of the most exciting Silicon Valley-based electric vehicle (EV) companies transforming the way the world moves. They're not just building cars-they're shaping the future of transportation. If you're driven by bold ideas and want to be part of a high-energy team redefin
Posted 5 days ago | Updated 4 hours 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 7 hours ago