System Validation Engineer Jobs

Join a leading Medical Devices Company in San Diego as a Principal Mechanical Engineer. This 12+ month contract requires deep expertise in tool design, molding validation (IQ/OQ/PQ), and hands-on experience with parameters. You will independently solve complex technical problems and design compon...

Join our growing team in San Jose as a Senior Software Quality Engineer. You will develop and execute test strategies for complex medical device software, primarily using C++/C#. This role requires Agile/Scrum experience, test automation skills, and a passion for creating life-saving healthcare t...

Join a global R&D team in San Diego as a Senior Mechanical Engineer. You will value engineer and commercialize disposable infusion products, applying 5+ years of design experience. This role requires cross-functional leadership, expertise in medical device design controls, and a strong foundation...

Seeking a Systems Engineer in San Diego to lead product verification and reliability activities. You will manage requirements, validation planning, and systems integration for new hardware/software. Requires 5+ years of experience, a BS in Engineering, and expertise in Systems/Reliability Enginee...

Join our team in Tempe as a Quality Engineer, focusing on new product transfer from design to manufacturing. You will apply your 2-4 years of medical device experience and knowledge of FDA/ISO standards to resolve production issues and lead validation activities. This role involves cross-function...

Join a leading Medical Devices Company in Sparks, MD as an Inventory Worker. This 12-month contract role on 3rd shift involves shipping, receiving, and material handling with equipment like pallet jacks. The position requires strong attention to detail, physical stamina, and the ability to work i...

Join our team as a Laboratory Technician in Vernon Hills, supporting critical medical device R&D and process development. You will assist engineers with prototyping, testing, data collection, and analysis in a regulated FDA/ISO environment. This role is ideal for a detail-oriented team player wit...

Seeking a Senior Hardware Quality Engineer in Louisville, KY or Vernon Hills, IL. You will ensure FDA-regulated quality, support design control, and manage validations. A BS in Engineering and experience in medical device development are required. ASQ certification is a strong plus.

Join ZebraSci in Temecula as a Mechanical Engineering Technician. Develop and validate test methods for innovative drug delivery systems and combination products. Utilize your expertise in mechanical testing, statistical analysis, and GMP/ISO standards within a dynamic engineering team.

Seeking an experienced Operations Manager for a Part 145 MRO in Abu Dhabi/Dubai. You will lead daily aircraft maintenance operations, ensuring technical performance, safety, and compliance with GCAA/EASA regulations. The role requires 8+ years in aviation, including 3+ years in management, and a ...

Seeking a Senior Hardware Quality Engineer in Louisville. This role supports quality assurance and design control for medical devices within an FDA-regulated environment. Ideal candidates have a BS in Engineering, 1+ years of industry experience, and strong knowledge of validation protocols and r...

Join a leading Medical Devices Company in Tempe, AZ, as an Engineering Technician. This contract role involves assisting with product builds, process development, and documentation for medical devices. The ideal candidate has 0-3 years' experience, can operate lab equipment, and holds a High Scho...

Join our San Diego team as a Quality Engineer II, specializing in validation for medical devices. You will execute IQ/OQ/PQ protocols, ensure ISO 13485 compliance, and manage nonconformances. The role requires 3-5 years in Pharma/Biotech, strong technical writing, and expertise in quality systems...

Join our R&D team as a Product Development Engineer in Franklin Lakes. This hybrid role requires 3+ years of medical device packaging experience, including design, prototyping, and V&V. You will apply your CAD and statistical expertise to develop compliant packaging solutions. Support innovation ...

Join a leading Medical Devices company as a Senior R&D Engineer on a 12+ month contract in Salt Lake City. You will drive product development using design control, GD&T, and validation (IQ/OQ/PQ) for high-volume manufacturing. The role requires a BS/MS in Engineering, 3+ years of experience, and ...

Join our team in San Jose as a Systems Verification Engineer II for flow cytometry products. You will verify product design, conduct experiments, and analyze system performance. This role requires a Bachelor's degree and 2+ years of product development experience. Apply your skills in a regulated...

Join our team in Mannford, OK as a Quality Engineer. You will ensure product quality and compliance with FDA/ISO standards in the medical device/pharma sector. Key duties include validation, statistical analysis, and cross-functional collaboration. A BS degree and 2+ years of GMP experience are r...

Join our team as a Quality Engineer in Covington, USA. You will ensure product and service quality through validation, statistical analysis, and cross-functional collaboration. This role requires basic FDA/ISO knowledge and experience with test protocols. US Citizenship or Green Card is mandatory.

Join our team in San Jose as a Senior Software Quality Engineer. Lead test strategy, automation, and a small team for complex software systems. Requires 6+ years of experience, cybersecurity testing knowledge, and strong leadership skills. ASQ certification is a plus.

Seeking an experienced Construction Manager in Montreal to lead institutional projects for Enclos Tensile Structures. This green job requires a Civil Engineering degree, 5+ years in ICI construction, and proficiency in Primavera, Rhino, and AutoCAD. We offer a supportive environment with paid tim...