About the role
AI summarisedThe Staff Systems Engineer supports New Product Introduction and on-market activities for genetic analysis instruments, serving as a technical bridge between Instrument Operations and product development teams in Singapore and the US. The role involves hands-on system failure analysis, characterization, and process improvement, with leadership in test process deployment, root cause analysis, and cross-functional collaboration to ensure system requirements are met. Responsibilities include driving operational excellence, writing work instructions, and supporting engineering studies to sustain high-performance standards throughout the product lifecycle.
BiotechOnsite
Key Responsibilities
- Lead and drive the deployment and continuous improvement of test processes and strategies to ensure system level requirements are met, including managing test specification changes throughout the product lifecycle
- Represent Instrument Operations and engage early with development teams to understand system level design and interactions across optics, fluidics, motion system, and advanced image sensors/cameras for cutting-edge genetic analysis instruments
- Lead and coach system-level debugging and drive root cause analysis for hardware, firmware, software, and chemistry/reagent related issues on complex systems (e.g.
- Instruments with optical & fluidics sub-systems) and provides technical recommendations
- Diagnose system level issues and develop hypotheses based on observed failures
- Perform and coach structured root-cause analysis for complex production issues using systematic problem-solving methodologies (FMEA, DOE, and statistical analysis)
- Complete Non-conformance Records based on investigation outcomes and drive release of instruments back into production
- Establish engineering studies to support various experiments and data collection efforts
- Participate in continuous improvement initiatives and operational excellence programs
- Write and update work instructions as needed to improve test procedures
Requirements
- Typically requires a minimum of 8 years of related experience with a Bachelor’s Degree; or 6 years and a Master’s Degree; or a PhD with 3 years’ experience; or equivalent experience
- Strong analytical foundation with solid understanding of statistical analysis and critical thinking skill, supported by experience using data analytics to drive decision making
- Experience in explaining and presenting complex technical issues to audiences with different backgrounds and provide sound technical recommendation and direction
- Experience developing scripts to extract/debug information from embedded systems and high-performing compute system running Oracle Linux
- Proficient in statistical analysis tools (i.e: JMP) for test data analysis, and requirement/test management tools (i.e: JAMA)
- Experienced in specification characterization and driving system performance robustness
- Excellent team player, interpersonal and communication skills
- Willing to travel to US for extended periods to learn the technology and collaborate with the US design teams
- Strong working knowledge of GDP, ISO & cGMP practices
- Experience with FDA regulated medical device product development preferred
- Experience in life science–related projects or internships is advantageous; exposure to medical device environments is preferred
- Familiarity with DNA sequencing, microarray platforms, liquid handling robotics, and system-level testing (hardware, firmware, software, and chemistry/reagents) is highly desirable
- Experience with Linux system will be a plus