Manufacturing Engineer III

Job Title Manufacturing Engineer III Essential Functions and Responsibilities Manufacturing Engineer III for Cincinnati, OH to lead provision of engineering support for new product development projects; coordinate & prioritize engineering tasks and milestones; lead process validations; manage large-scale legacy projects from initiation to implementation; prepare design requirements; execute product transfers; support engineering evaluation & analysis of product quality issues; assure engineering changes & product designs adhere to applicable regulatory, safety & design standards; create & maintain product engineering documentation; lead execution of product & process improvements; serve as subject matter expert for change control & product design and development processes; mentor & train junior engineers. Requires Master’s in Manufacturing or Industrial Engineering or closely-related field & 2 yrs experience using Microsoft Project and/or Excel to track engineering project tasks, deliverables and milestones; designing & developing medical devices within cGMP & regulatory standards; maintaining & revising DHR and DHF documents; applying GD&T to product designs; reading engineering drawings & prints; working with heat transfer properties & thermal management systems; using Visual CRM software; working with third-party test agencies; supporting external regulatory audits; performing engineering change control; performing root cause analysis & engineering change control; performing medical device process validation, including installation, operational & performance qualification, in alignment with ISO 13485 standards. Minimum Qualifications Requires Master’s in Manufacturing or Industrial Engineering or closely-related field & 2 yrs experience using Microsoft Project and/or Excel to track engineering project tasks, deliverables and milestones; designing & developing medical devices within cGMP & regulatory standards; maintaining & revising DHR and DHF documents; applying GD&T to product designs; reading engineering drawings & prints; working with heat transfer properties & thermal management systems; using Visual CRM software; working with third-party test agencies; supporting external regulatory audits; performing engineering change control; performing root cause analysis & engineering change control; performing medical device process validation, including installation, operational & performance qualification, in alignment with ISO13485 standards. Equal Opportunity Statement Gentherm is an Equal Opportunity Employer. We are committed to building an inclusive culture through Our Network of Engagement (ONE) where we value our differences and work together to positively impact the lives of our employees, customers, and communities. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, genetic information, sexual orientation, gender identity, disability, or protected veteran status. Country/Region: US Nearest Major Market: Cincinnati Job Segment: Thermal Engineering, Medical Device, Medical Device Engineer, Manufacturing Engineer, Industrial Engineer, Engineering, Healthcare #J-18808-Ljbffr