Biomedical Engineer II

About the role

We anticipate the application window for this opening will close on 15 Jul 2026. At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.

Responsibilities

• Designs, develops, and evaluates electrochemical CGM, learning and applying foundational electrochemical and biomedical engineering principles to inform design decisions and understand how design parameters affect sensor performance.
• Applies & instills Best-Known-Methods for robust characterization of various sensor signals and performance outputs.
• Applies data analysis and statistical methodologies to generate insights on sensor performance, drive experiment design and project next steps.
• Conducts design of experiments (DOE) to model the statistically significant critical to quality (CTQ) sensor performance output variability and main effects with respect to process and environmental inputs.
• Utilizes technical skills associated with Six Sigma, Lean, DRM/DFSS and other appropriate continuous improvement techniques.
• Maintains accurate and complete laboratory records, experimental documentation, and data analysis reports in compliance with applicable quality system requirements and design controls.
• Contributes to the completion of project milestones under the guidance of senior members of the team, developing technical depth and breadth through mentored project work.

Requirements

• Bachelor’s degree with 2+ years of relevant experience; or advanced degree with 0+ years of relevant experience.
• Hands-on laboratory experience with electrochemical wearable biosensors, CGM, or related medical device systems.
• Familiarity with statistical software tools such as Minitab or JMP for experimental data analysis and visualization.
• Demonstrated ability to work both independently and within a team-based project environment.
• Direct experience with technical documentation including laboratory notebooks, engineering reports, standard operating procedures, and test protocols.
• Experience working with vendors, material suppliers, and equipment manufacturers.
• Familiarity with quality system requirements, design controls, and good laboratory practices in a regulated medical device or cGMP environment.
• Demonstrated written and verbal communication skills, with the ability to present experimental results and analytical findings clearly to project teams.