Vesta, part of Lubrizol LifeSciences, offers custom medical manufacturing services, including precision thermoplastic and silicone extrusion as well as comprehensive silicone fabrication from its ISO 13485 certified facilities. Vesta capitalizes on more than 40 years’ experience, leveraging expertise in design assistance, material selection and quality compliance to enable our customer’s success.
Vesta has served as a trusted medical device outsourcing partner for four decades, delivering innovative solutions in molding, extrusion and assembly. Our Franklin, Wisconsin location includes ISO 7 certified clean room, ISO 8 controlled environment, 116,000 ft2 (10,700 m2), 17 extruders with 12 lines, 75 molding presses and a dedicated R&D laboratory. Every one of our medical device manufacturing, assembly and support services has quality at its core. Our highly collaborative, end-to-end, medical device process validation ensures quality without sacrificing product performance.
The Quality Systems Engineer is primarily responsible for assuring Quality Systems quality compliance through the development, implementation, improving and monitoring of appropriate processes to meet quality/business metrics and goals. Specifically, the Systems Engineer is the process owner for different quality systems (CAPA program, customer complaints, nonconformance, internal and external audits, risk management and so forth).
DESCRIPTION OF ESSENTIAL DUTIES:
CONSIDERED A PLUS: