Senior Systems Integration Engineer – I – II – III
| Company | Cellares |
|---|---|
| Location | San Bruno, CA, USA |
| Salary | $90000 – $210000 |
| Type | Full-Time |
| Degrees | Bachelor’s, Master’s, PhD |
| Experience Level | Senior |
Requirements
- BS in Engineering, Bioengineering, Physics, or related field with 5+ years of extensive, hands-on experience in developing analytical instrumentation and biotech automation
- OR MS or PhD in Engineering, Bioengineering, Physics, or related field with 3+ years of extensive, hands-on experience in developing analytical instrumentation and biotech automation
- Extensive hands-on experience in integration testing and troubleshooting in highly complex instrumentation systems that combine fluidic handling, electronic sensors, gas mixing, and robotics
- Hands-on experience with autologous and allogeneic cell therapy manufacturing processes is a plus
- Experience with scripting languages (MATLAB, Python, JMP, etc.) for modeling, simulation, and data processing
- Prior experience with ISO regulations, cGMP, QMS, and IEC 61010 standards is preferred
- Excellent verbal, written, presentation, and interpersonal skills
- Strong analytical and problem-solving mindset
- Self-awareness, integrity, authenticity, and a growth mindset
Responsibilities
- Technical lead to perform hands-on system characterization, integration, verification testing, troubleshooting, root-cause investigation, and continuous improvement of Cellares technology platforms
- Work closely with the Hardware, Software, Firmware, Process, and Manufacturing teams to perform system characterization, testing, and continuous system improvement
- Design and execute complex experiments, following scientific principles and statistical approaches, to support the development and characterization of customer processes
- Author and present quality technical documents, procedures, and reports
- Produce technical reference documentation and reports, and provide training and assistance for the operations team
- Interface closely and actively with cross-functional teams, and self-motivated to drive given tasks to completion
Preferred Qualifications
- Hands-on experience with autologous and allogeneic cell therapy manufacturing processes is a plus
- Prior experience with ISO regulations, cGMP, QMS, and IEC 61010 standards is preferred