Position Overview
Responsibilities:
Demonstrate creative 'out of the box' thinking to solve difficult problems and develop new technologies to achieve project goals.
Design and execute design of experiments and fixture development to support feasibility, development, and verification stages of product development to meet project timelines and all relevant regulatory compliance requirements.
Define, develop, and validate/transfer test methods.
Create verification plans, protocols, records, and reports. Support investigations and issue resolutions. Requirements: A degree in an engineering field (mechanical, materials, packaging, bioengineering): BS or equivalent education with - years of experience; MS or equivalent education with + years of experience.
Strong expertise in Design Verification for Medical Devices and experience working in a regulated environment in compliance to CFR and MDR.
Signific...