Cellares
Automation Engineer (I, II, III)
About this role
Join a mission-driven team developing automated QC testing systems for a cell therapy platform in a regulated GMP environment. This role combines hands-on operational support with method development and optimization across multiple automated workcells in Bridgewater, NJ.
What you'll do
- Develop, validate, and operate fully automated QC testing workflows in GMP-regulated environment
- Transfer and scale automated QC test methods across multiple workcells
- Troubleshoot automation systems and provide runtime operational support
- Design and implement automated sample and reagent management workflows
- Support system validation, user training, and technical documentation
- Maintain change control and version management of automated test methods
What they're looking for
- Laboratory automation and workcell operation
- QC testing and analytical methods
- GMP/regulated environment compliance
- System troubleshooting and problem-solving
- Technical documentation and change control
- Cross-functional collaboration
- Sample and reagent management
- User training and communication
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Cellares
Cellares builds automated systems and platforms for cell therapy manufacturing and quality control testing. The company is hiring Process Engineers, Automation Equipment Engineers, and Lab Systems Engineers to design, optimize, and maintain manufacturing workflows and automated workcells in a regulated biotech environment.
- Website
- cellares.com
Likely interview questions
- Describe your experience developing or supporting automated testing workflows in a regulated (GMP/FDA) environment. What compliance or validation challenges have you encountered?
- Walk us through how you've troubleshot a failing automated system in production. What was your approach and what tools or methodologies did you use?