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10 часов назад

Automation Equipment Engineer (I, II, III)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle/senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Automation Equipment Engineer (I, II, III) (Cell Therapy Manufacturing): Troubleshooting and sustaining automation equipment and control systems for an advanced cell therapy manufacturing platform with an accent on PLCs, sensors, motors, pumps, pneumatic actuators, articulated robots, and software interfaces. Focus on diagnosing production issues, commissioning and validating automation changes, developing operational runbooks, and feeding recurring equipment problems back into permanent R&D improvements.

Location: South San Francisco, California, United States. On-site, full-time third-shift role with nights and/or weekends; occasional travel of less than 15% may be required.

Company

hirify.global develops an advanced cell therapy manufacturing platform supported by automated equipment and control systems.

What you will do

  • Monitor equipment fleet health, maintain readiness, respond to production issues, and support proactive testing.
  • Troubleshoot sensors, motors, pumps, pneumatic actuators, PLC logic, six-axis robots, and software interfaces.
  • Identify recurring equipment issues and improvement opportunities, and provide feedback to the R&D team.
  • Develop and maintain runbooks, troubleshooting guides, and operational procedures.
  • Coach operators and technicians on control-system questions and support commissioning and validation of automation changes and new systems.

Requirements

  • Bachelor's degree in Electrical, Mechatronics, Systems, or Process Engineering, or equivalent experience.
  • At least 2 years of experience supporting automated production equipment, preferably in medical device or pharmaceutical manufacturing.
  • Hands-on experience wiring, configuring, and verifying electrical and control systems.
  • Working knowledge of EtherCAT, Modbus TCP/IP, serial interfaces, and OPC-UA; ability to read P&IDs, electrical schematics, and technical drawings.
  • Experience reading IEC 61131-3 Structured Text, working with a major PLC platform, and supporting integrated articulated robots.
  • Experience in a GMP or similarly regulated environment, including change control, deviation, and CAPA processes; willingness to work off-shift schedules.

Nice to have

  • Production experience with Beckhoff TwinCAT 3 and TwinSAFE.
  • Experience with HMI or SCADA platforms such as Ignition, Wonderware, or WinCC.
  • Familiarity with InfluxDB, Grafana, Git, Python, or other scripting tools.
  • Experience with cell therapy, biotech, semiconductor, or other high-mix automated manufacturing platforms.

Culture & Benefits

  • Fast-paced, mission-driven environment focused on cell therapy manufacturing.
  • Hands-on technical ownership bridging operations and engineering.
  • Collaboration with operators, scientists, engineers, and R&D teams.
  • Leveling is based on overall experience, education, and demonstrated knowledge during the interview process.

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