automation-engineering jobs in San Diego

Senior Automation Engineer supporting the development, maintenance, and operation of complex custom automation systems in a biotech environment. Responsibilities include understanding system requirements, developing scripted protocols, supporting system integration across hardware and software, troubleshooting failures, and ensuring compliance with FDA regulations and GxP principles.…See more The role requires proficiency in C#, experience with robotics, motion control, machine vision, and strong problem-solving skills to maintain system uptime in a regulated biotech setting.

The Senior Automation Engineer will develop, maintain, and troubleshoot complex custom automation systems for biotech applications, with a focus on hardware–software integration and regulatory compliance. Responsibilities include writing operational protocols, performing system integration, conducting verification and validation testing, and collaborating across cross-functional teams.…See more The role requires a strong foundation in automation engineering principles, C# proficiency, hands-on experience with robotics, motion control, sensors, and machine vision, plus familiarity with FDA regulations (21 CFR Parts 11, 210, 211, 820) and GxP principles.

Senior Automation Engineer at a biotech firm developing autologous stem-cell therapies. Responsible for developing, maintaining, and troubleshooting complex custom automation systems, including scripted protocols, hardware-software integration, and verification/validation testing.…See more Requires 5+ years in hardware design, automation, or biotech, with strong C# software integration skills, robotics and motion control expertise, and knowledge of FDA regulations (21 CFR 11, 210, 211, 820) and GxP principles.

The Senior Automation Engineer will develop, maintain, and troubleshoot complex custom automation systems in a biotech setting, working with hardware (robotics, motion platforms, sensors, machine vision) and software (C# codebases). Responsibilities include creating operational protocols, supporting system integration, developing verification and validation plans, and ensuring compliance with FDA regulations (21 CFR Parts 11, 210, 211, 820) and GxP principles.…See more The role requires 5+ years in hardware design, automation, or biotechnology, with strong problem-solving skills and the ability to collaborate across cross-functional teams.