Validation Engineer III
ManpowerGroup Global, Inc.
Our client, a leader in the medical device industry, is seeking a Validation Engineer III to join their team. As a Validation Engineer III, you will be part of the Quality Assurance Department supporting validation activities across multiple projects. The ideal candidate will demonstrate strong technical expertise, excellent communication skills, and a proactive approach to problem‑solving, which will align successfully within the organization. Job Title: Validation Engineer III Location: San Diego, CA Pay Range: $39/hr on w2 What's the Job? Lead and execute validation protocols for equipment, processes, and systems in compliance with FDA, ISO 13485, and other relevant standards. Develop and maintain validation documentation including URS, FRS, DRS, FAT, DQ, IQ, OQ, PQ, PV, and related reports. Perform risk assessments, gap analyses, and support continuous improvement initiatives within the Quality Management System. Support internal and external audits by providing validation documentation and technical expertise. Manage validation projects, develop timelines, and communicate project status to stakeholders effectively. What's Needed? Bachelor's degree in Engineering, Biology, Chemistry, or a related science field. At least 5 years of experience in validation within the medical device or related industry. Proficiency in equipment qualification (IQ/OQ/PQ), process validation, and computer system validation. Strong understanding of FDA regulations, ISO standards, and Good Documentation Practices. Excellent problem‑solving, organizational, and communication skills, with the ability to work independently and collaboratively. What's in it for me? Opportunity to work in a dynamic, innovative environment supporting life‑changing diagnostics. Chance to contribute to high‑quality validation processes and ensure compliance with industry standards. Collaborate with a diverse team of experts committed to excellence and continuous improvement. Engage in meaningful projects that impact patient health and safety. Be part of a company that values diversity, inclusion, and professional growth. If this is a role that interests you and you would like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! #J-18808-Ljbffr
$101.55k - $132.4k
...Validation Engineer 2 (Req# IIC1539) in San Diego, CA. Telecommute permitted within area of intended employ. Coord w/end users & process owners to lead dvlpmt of validation strategy for proj, sys & processes.BS+3yrs rltd exp. $101,546 $132,400/yr. Email resumes to Illumina...SuggestedRemote work$87k - $103k
...generate potentially transformative therapies. For more information, visit Position Summary Artiva Biotherapeutics is seeking a Validation Engineer II to support qualification and validation activities for GMP facilities, utilities, equipment, computerized systems, and...SuggestedFull timeMonday to FridayFlexible hours$171.6k - $302.2k
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Silicon Validation Software Engineer- GPU IP Validation and Integration Do you love creating elegant solutions to highly complex challenges? Do you intrinsically see the importance in every detail? As part of our Silicon Technologies group, you’ll help design and manufacture...Relocation$130k - $165k
...Sigma Defense is seeking a Systems Engineer II-III to join our team in San Diego NB, CA. Equal Opportunity Employer/Veterans/Disabled:... ...Experience with requirements development, verification, and validation. Experience supporting installation, certification, operational...- Apple Inc. is seeking a Software Engineer for SoC Level Validation Engineering in San Diego, California. This role involves writing tests, debugging, and maintaining system-level software to ensure high-quality Apple products. The candidate should have a Bachelor's degree...
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Apple Inc. is seeking a Design Verification Engineer to verify complex Wireless SOCs in San Diego. You will be integral to the verification effort and responsible for pre-silicon RTL verification, focused on high Efficiency SOC architecture and wireless protocol requirements...- ...company developing next‑generation cell and gene therapies. In this on‑site contract role, you’ll lead and enhance the Computer System Validation (CSV) program, ensuring compliance across laboratories, manufacturing, and quality systems. What You’ll Do Serve as the site CSV...Contract work
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