Description :
The Senior Quality Engineer applies best practices from within the field of quality control to ensure that the materials, components, processes, and manufacturing techniques used produce high quality and reliable products. Nature of Role: T his go-to resource stays abreast of current quality and regulatory trends and ensure s the successful integration of quality assurance and regulatory compliance, working across multiple teams and medical device/equipment categories Requirements: Bachelor's degree in a scientific or engineering field is required Experience in a quality engineering role in the medical, electronics packaging, high reli ability, or a related industry Previous experience with manufacturing and assembly processes is required Strong written and verbal communication skills are required, including proficiency with standard office productivity sui te and data analysis software ISO Lead Auditor training is preferred Experience operating in compliance with ISO:1348 5 and FDA regulated environment Experience working in an environment where employees are empowered to bring new ideas and suggestions in support of business process improvement Responsibilities: Plans, executes or directs activities concerned with development, application, and maintenance of quality standards. Reports results to marketing, manufacturing, process enginee ring, and product design groups Develops and initiates standards and methods for inspection, testing, and evaluation, utilizing knowledge in engineering fields suc h as electrical, or mechanical Establishes programs to evaluate analytical testing, equipment, facilities, precision measurements, accuracy measurements, and performance testing Coaches and directs workers engaged in measuring, testing, and tabulating data conc erning quality and reliability Manages measurement calibration program, including verification of internal comp liance to calibration program Perform factory floor audits of finished products, manufacturing and test procedures, and document control compliance Lead or assist in quality evaluation of returned products and support RMA program Lead, participate in, or coordinate Internal Corrective Action initiatives Compiles and writes training material and conducts training sessions on quality control activities