Job Title: Validation Engineer
Experience: 4 - 5 years
Location: San Jose, CA, USA
Education: Bachelor of Science in Engineering, B.E. / B.Tech. Mechanical Engineering, M.S. Mechanical Engineering

Experience Requirements:

• Minimum 3 years of relevant experience in Medical Device Manufacturing.
• Experience working in a clean room environment.
• Experience with Test Method Validation and/or Measurement System Analysis is preferred.
• Knowledge of computer software for data analysis, specifically Microsoft Excel and statistical packages (Minitab preferred), is a plus.
• Demonstrated understanding of FDA Quality System Regulation (21 CFR 820) and ISO 13485.
• Strong organizational skills and detail-oriented.
• Proficiency in Microsoft Office, including Microsoft Word, Excel, and PowerPoint.
• Experience with 3D CAD Software SolidWorks.
• Experience working with Engineering change management software and releasing engineering change orders.

Job Duties:

• Process and equipment qualification (IQ/OQ/PQ).
• Development of test methods for Design Verification & Validation (V&V), Process Validation, and Production.
• Validation of test methods.
• Execution of Engineering Builds, Gauge R&R Studies, Attribute Analysis Studies, and other validation work.
• Authoring/releasing new test methods and editing/redlining old test methods.
• Experience working in a regulated and/or medical device environment.
• Defining equipment requirements.
• Drafting equipment specifications.
• Working on change management and releasing engineering change orders.
• Designing process validations and identifying critical process parameters related to equipment.