Bioengineer I/II

Department

Bioengineering

Location

San Diego, California

Job Type

Full-Time

ID #

1234578


Cue Health Inc. is seeking to hire a full-time Bioengineer I/II with expertise in design and development of medical diagnostic instrumentation or similar. This position is hands-on and requires a varied skill set with a natural aptitude for continuous improvement.

Responsibilities:

  • Specify, design, test and support medical diagnostic products (lab-on-a-chip platform)

  • Exercise considerable judgment and take initiative required to resolve problems and make recommendations

  • Work on teams to develop and transfer new processes/products to production and enhance their robustness

  • Work cross functionally with R&D, Manufacturing and Quality to develop processes for new products and improve processes of existing products

  • Construct and execute controlled experiments to optimize processes, address yield and quality issues and drive implementation of solutions in a regulated production environment

  • Document experimental data, present data, write test reports

  • Adhere to established protocols and good laboratory practices while meeting expected daily and weekly deliverables

  • Install, qualify (IQ/OQ/PQ), maintain and debug platforms that are in development

 


Requirements:

  • Degree in Bioengineering, Mechanical Engineering, Biology, or related field

  • BS with 2+/5+years’ experience, or MS with 0+/3+ years’ experience

  • Ability to debug system-level issues that involve instrumentation, microfluidics, chemistry and software, and offer cost-effective, expedient solutions

  • Ability to generate technical documentation with attention to detail

  • Excellent written and verbal communication skills

  • Self-motivated to lead projects while working effectively in a team

  • IVD experience is a plus

  • Knowledge of SolidWorks, JMP, and/or programming languages such as Python is a plus

  • Experience with statistics, Statistical Process Control, and DOE techniques is a plus

  • Experience in process development, validation, and implementation is a plus

  • Experience with FDA QSR (quality system regulations) and structured product development (i.e., design controls) is a plus

  • Knowledge of GMP and GDP lab practices is a plus