valid

Stellantis is seeking an EE Validation Project Chief (VPC) to lead and coordinate electrical system validation activities across vehicle programs. The VPC ensures project development aligns with quality, timing, and cost objectives while maintaining compliance with technical requirements. This role serves as the primary interface between the EE Validation &...

Position Summary The Validation Engineer II is responsible for the design, scheduling, execution, and evaluation of scientifically and statistically sound qualification and validation studies. This role demonstrates that critical cleaning, controls, equipment, facilities, processes, and utilities function consistently and repeatably in compliance with...

We are looking for a contract to hire Validation Engineer to join our medical device manufacturing client in Southeastern Wisconsin! This position is responsible for writing, implementing, analyzing results and summarizing process validation activities in the areas of equipment installation, change management, and continuous lifecycle improvement. This...

JOB DUTIES:• In this role, this engineer will be part of a highly technical team that develops test plans, completes functional & electrical validation, & debugs issues for new processor silicon interface features with strong focus on power management. • Writes comprehensive electrical & functional test plans for the processor interface validation of...

# Validation DirectorAUBURN HILLS HQ R&D, US-MI, United StatesID: 67687---## Job Description## **Forvia, a sustainable mobility technology leader**We pioneer technology for mobility experience that matter to people.## **Your mission, roles and responsibilities**The Director of Validation leads the NAO validation organization and is responsible for defining...

Pfizer is seeking a senior Quality Assurance professional to evaluate validation master plans, protocols, and reports in a penicillin facility. The role covers troubleshooting, data analysis, process validation, and regulatory audits, with responsibilities across documentation, change control, and quality systems. Applicants must meet rigorous GMP standards...

Stellantis is seeking aSystem Analyst Validation Engineer (VST)who will be responsible for understanding the development, design, and interactions of electrical and electronic systems within vehicles, including automotive body, audio, active chassis, and/or safety systems. The engineer will be responsible for developing and leading automated stress testing...

Position Summary We are seeking a detail-oriented Validation Specialist to support validation and qualification activities within a pharmaceutical manufacturing environment. This individual will help ensure that manufacturing equipment, utilities, facilities, computerized systems, and processes are qualified and validated in accordance with applicable...

Job Title: Technical Director – Validation Location: Johns Creek, GA – Hybrid (3 days onsite) Salary: $160,700 – $298,400 + bonus & equity A leading semiconductor company is looking for a Technical Director – Validation to join its Memory Interface team. This is a senior, hands‑on role focused on silicon validation, high-speed memory interfaces and...

Position Summary We are seeking a detail-oriented Validation Specialist to support validation and qualification activities within a pharmaceutical manufacturing environment. This individual will help ensure that manufacturing equipment, utilities, facilities, computerized systems, and processes are qualified and validated in accordance with applicable...

HonorVet Technologies is a Service Disable Veteran-Owned IT staffing firm, ISO 9001, and ISO 27001 certified, working with federal agencies, state governments, and Fortune 500 enterprise clients across the US. What makes us different isn't a tagline; it's the way we work. We don't forward resumes and hope for the best. We take the time to understand where a...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of...

Job Summary Under general supervision, plan and execute verification and validation activities. Ensure regulatory compliance by inspecting, measuring, analyzing, auditing, calibrating and testing instrumentation, equipment, software/hardware, machines and/or procedures. Identify problems and their sources and correct them quickly and efficiently. Implement...

3key Consulting, Inc. in Cambridge, MA is seeking an Engineer – GMP Test Methods Development & Validation for a 2+ year contract with potential extensions. The role focuses on development, validation, and lifecycle management of physical test methods and associated equipment within a regulated biopharmaceutical setting. The ideal candidate will have strong...

Zebra Technologies Corporation is seeking an Engineering Technician II in the United States to independently perform hardware testing and support product validation. You will operate a range of test equipment, troubleshoot issues, and coordinate with engineering on testing deliverables to ensure quality and performance. The role emphasizes reading...

Job Title: Senior Validation CQV Engineer Experience: 9+ Years Industry: Pharmaceutical / Biotechnology Position Summary : We are seeking an experienced Senior Validation CQV Engineer with 9+ years of experience in pharmaceutical or biotechnology environments to support a facility expansion and upgrade project in California. The ideal candidate will have...

K2 Space is seeking a hands-on SerDes Characterization & Post-Silicon Validation Engineer to bring up and characterize high-speed SerDes interfaces in complex SoCs. You will work closely with SerDes/IP, mixed-signal, digital, firmware, SI/PI, package, board, and systems teams to take high-speed interfaces from first silicon through product integration and...

i-Pharm GxP in Lebanon, Indiana is seeking a Senior CQV Engineer to join a major peptide API manufacturing capital program. The role is hands-on, field-based, and requires strong experience delivering commissioning, qualification and validation from construction through handover. Responsibilities include IQ/OQ/PQ protocol development, P&ID walkdowns, and...

cGMP Consulting Inc. seeks an experienced senior leader to manage multiple validation and qualification projects across equipment, utilities, facilities, systems, and processes in a GMP environment. The role offers significant autonomy and cross-functional leadership to influence operations in a fast-paced, regulated manufacturing setting. The ideal...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of...