• Job Description

  Req#: 26983721-1011-4540-839d-05f5eb924cf7

  We are seeking an innovative and highly motivated controls engineer who will make significant contributions to the development of our advanced cell therapy manufacturing platform.

  
  

  The primary focus of this position will be the design, implementation, and test/verification of control systems that form the core of our hardware platform. You will lead the development of control systems for these hardware platforms and collaborate with the software, mechanical, and systems teams to bring up and validate new automation systems. You will interface with various parts of the company to develop novel products used in the cell therapy and gene therapy fields.

  
  

  Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company scales up from R&D systems to full-scale operations.

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  Responsibilities

  • Lead the development of control systems integrating custom and off-the-shelf laboratory instruments, PLC-based control hardware, and articulated robots
  • Drive component selection, prototyping, bring-up, debugging, documentation, manufacturing, and testing
  • Develop PLC control software using Structured Text and leverage object-oriented programming methodologies
  • Develop articulated robot control software using Staubli Robotics Suite
  • Develop unit tests and functional tests for PLC and robotics code that you write, participate in code reviews, and leverage Git for version control and code management

  • Participate in design reviews and provide input to identify issues and drive design choices
  • Collaborate cross-functionally, including with Systems Engineering, Mechanical Engineering, Quality, and Process Development for project planning, requirements development, and architecture development
  • Collaborate with the software team to develop robust, well-documented software interfaces to hardware
  • Collaborate with external suppliers and contract manufacturers
  • Develop test software in Python, C#, or other languages to validate subsystems during manufacture

  
  

  Requirements

  • Bachelor's or Master's degree in Electrical Engineering, Mechatronics Engineering, Computer Engineering, Computer Science, Software Engineering, or equivalent experience is required
  • 5+ years industry experience developing control systems for customer-shippable life science instruments or comparable equipment
  • 2+ years of experience in medical device design preferred
  • Experience integrating and/or programming industrial articulated robots (i.e., Staubli, FANUC, Kuka, ABB)
  • Experience with at least one major PLC platform (Beckhoff TwinCAT, Siemens TIA Portal, B&R) or experience with hardware control using real-time operating systems (RTOS) such as VXWorks, QNX, INtime, etc.
  • Proficient with IEC 61131-3 based languages with a focus on Structured Text
  • Proficient with object-oriented programming and have an understanding of how to apply OOP concepts to control software

  • Experience with fieldbus technologies, including EtherCAT, Profinet, EtherNet/IP, and Modbus.
  • Experience implementing and developing coding standards around industry standard control implementations, for example, implementations following the ISA-88 hierarchical model
  • Experience reading and interpreting electrical drawings
  • Hands-on experience with wiring, configuring, and troubleshooting electrical and control systems
  • Proficient in the design of safety systems following IEC/ISO/RIA standards
  • Understanding of the proper integration and usage of safety relays, safety PLCs, light curtains, E-Stops, etc
  • Experience with one computer programming language such as Python, C#, Java
  • Desire to work in a fast-paced, collaborative start-up environment
  • Self-awareness, integrity, authenticity, and a growth mindset

  
  

  Nice to Haves

  
  

  • Proficiency in Python
  • Experience with at least one major HMI software, such as Ignition, Wonderware, WinCC
  • Comfortable leveraging AI tools to accelerate development

  
  

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  $90,000 - $210,000 a year

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  This is Cellares

  
  

  Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.

  The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

  
  

  Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

  
  

• About the company

  Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patient...

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