Automation Engineer (I, II, III)

Cellares•Bridgewater, NJ

5d•$90,000 - $210,000•Onsite

About The Position

We are seeking an Automation Engineer to support the development, validation, and day-to-day operation of fully automated QC testing workflows in a regulated GMP environment at our Bridgewater, NJ site. This role is central to the success of our Cell Q platform and commercial-scale QC operations. The successful candidate will play a key role in transferring, scaling, and optimizing automated QC test methods across multiple automated workcells, while also providing hands-on runtime operational support for the Cell Q platform and the broader QC laboratory infrastructure. This includes troubleshooting systems, supporting production testing, and ensuring consistent, compliant execution of automated workflows. Working closely with cross-functional partners in Quality Control, Analytical Development, Manufacturing, IT, and Quality, the Automation Engineer will contribute to system validation, user training, technical documentation, and controlled version management of automated test methods under change control. In addition, this role will help design, implement, and maintain automated sample and reagent management workflows that enable scalable, reliable, and robust end-to-end processes for high-throughput QC testing in a GMP setting. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad range of challenges as the company grows.

Requirements

Bachelor's or higher degree in Engineering, Computer Science, Biotechnology, or a related field
2+ years of experience designing, implementing, and maintaining laboratory automation systems.
Experience programming and optimizing liquid handling methods
Experience developing and implementing integrated automation solutions using Bioseroâs Green Button Go software
Experience with laboratory analytical instruments and automated systems
Experience integrating and managing assay results with LIMS
Familiar with flow cytometry, genomic, and cell-based assays
Strong technical writing skills and experience authoring Standard Operating Procedures (SOPs), documentation, and training materials
Excellent problem-solving skills and the ability to troubleshoot technical issues.
Strong communication skills to collaborate effectively with cross-functional teams.
Attention to detail and the ability to work independently and manage multiple tasks simultaneously.
Creative, self-motivated, eager to take on a wide variety of tasks and grow with the evolving technology
Self-awareness, integrity, authenticity, and a growth mindset

Responsibilities

Support the transfer and validation of automated QC workflow steps
Validate and optimize automated methods for sample preparation, analysis, and data collection
Monitor system performance, track recurring issues, and collaborate with engineering and quality teams to implement technical and procedural improvements
Conduct validation testing of liquid handling methods and integrated systems to ensure proper functionality and performance
Analyze automation workflows to identify bottlenecks and areas for optimization
Develop and implement troubleshooting methodologies to identify and resolve QC test method issues
Provide automation system and instrumentation support and troubleshooting