Senior Quality Engineer - Remote

Overview

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFR_CT Analysis—provides a color-coded, 3D model of a patient’s coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFR_CT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare.

In Short

• Support frequent minor software releases by performing risk assessments and aiding regulatory teams in establishing better processes for risk management
• Collaborate with cross-functional teams to drive quality project management activities
• Manage audits (internal and external) and communicate non-conformities assessed to greater team, driving the implementation of change when needed
• Collaborate with external partners including regulatory agencies, authorized representatives, importers and distributors to support management of Quality Systems
• Provide input to the risk management process to ensure risks are identified and updated during the product life cycle
• Conduct Quality assessment of changes to standards and regulations and communicate cross-functionally
• Support and drive Quality System management and implementation of changes
• Support Corrective and Preventative Action (CAPA) processes and non-conformances (NCRs) through identification of root cause
• Train company in support of Quality initiatives
• Other relevant duties as assigned

Requirements

• Experience working with SaMD and AI / ML devices a must
• High competency of ISO 13485, ISO 14971, 21 CFR 820
• Experience with risk management activities including risk assessment and review of FMEAs
• Project management skills
• Demonstrated team collaboration
• Excellent communication, writing, and editing skills
• Strong Word, Excel, and PowerPoint skills
• Front room audit experience required.

Benefits

• Competitive salary and cash bonus
• Stock options
• Opportunities for professional development
• Work in an innovative and supportive environment
• Contribute to meaningful healthcare advancements