LifeLens Technologies Benefits Overview

Develops electrochemical medical devices from concept through regulatory clearance and commercialization. Responsibilities include prototyping, performance evaluation, design selection, risk management, design documentation, verification and validation testing, manufacturing support, and collaboration with manufacturing, quality, and regulatory teams. The role requires experience with Class II or III medical devices, Design Controls, international standards, experimental methods, prototyping, material characterization, and manufacturing equipment qualification.

Leads process development, validation, risk analysis, and continuous improvement for medical device manufacturing. Develops and validates stable production processes, conducts trials and DOE studies, evaluates materials and process changes, establishes acceptance criteria, and authors technical reports. Collaborates with Quality, R&D, engineers, and technicians while supporting manufacturing operations, implementing equipment safety protocols, and leading process improvement initiatives.