The Quality Engineer II is tasked with maintaining and analyzing quality systems to comply with FDA regulations and ISO 13485 standards. Responsibilities include conducting investigations, leading non-conformance investigations, participating in product qualification at suppliers, and implementing quality assurance testing models. This role collaborates with different departments to ensure quality standards are met and drives process improvements based on discrepancies.

The Systems Engineer at INOVIO will lead the design and development of medical devices, create user requirements, manage risk and traceability documentation, ensure regulatory compliance, and collaborate with cross-functional teams to finalize device designs.