Every day, Kelly Services connects professionals with opportunties to advance their careers. We are currently seeking a Quality Engineer, preferably with Medical Device experience to support Product Life Cycle Management activities and projects for our clients. Our client is very well known as one of the largest, most innovative medical device and solutions, in orthopaedics, spinal care and neuroscience, in the world today. This opportunity offers an enhanced benefits package from Kelly Services which includes 401K participation, health insurance, PTO, and paid holidays. Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. Applicants must be legally permitted to work in the United States immediately and without employer sponsorship (F1 OPT cannot be considered for this position). Duties: Concentration on CAPA activity. Assess the LCM projects and validations; provide risk assessments and remediation plans. Ensure projects remain on track and on schedule. Provide Technical Validation Engineering support to write, obtain approval, execute and close out assigned validation activities as required. Write, review and execute qualification and validation protocols on assigned pieces of equipment, processes and inspection devices. Support validation activities including Installation Qualification, Operational Qualification and Performance Qualification. Process and Equipment validations will include floor layout optimization meeting ergonomic design needs and Lean principles. Write, revise and gain approval for controlled documents such as completion reports, process specs, work instructions, training manuals and Process Failure Mode Effect Analysis. As requested support Quality System remediation activities. Required Qualifications: A minimum of a bachelor’s degree in Sciences, Business, Engineering or related technical field is required A minimum 2-3 y...