Investigating, planning and implementing medical product improvements and evaluate critical quality manufacturing processes that directly affect patient safety and product quality. Must successfully reduce defects of the clients devices and must aid in producing a better quality product more efficiently. Writing and executing physical and chemical test method protocols. Must adhere to quality policies like EU MDR, 21CFR820 set forth by FDA and respond to customer complaints, perform audits, developing test methods, validation etc.Travel and/or relocation to various unanticipated locations throughout the US may be required. Need Master's degree in Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering or related.