Manufacturing Engineer III

Your Career. Your Impact. Your Future.

At Gentherm, we believe the next big breakthrough begins with you. As a global leader in thermal management and pneumatic comfort technologies, we develop advanced systems that deliver meaningful solutions to enhance health, wellness, comfort, and efficiency in everyday life. Our products and innovations are created for you, by you.

Be part of our team where a human-centric mindset drives everything we do—from the technologies we build to the careers we support. With decades of expertise, we have pioneered advanced solutions that have become a standard expectation for consumers around the world.

The same thoughtful approach we take in developing our technologies guides how we support your career: purposeful, impactful, and tailored to you. Because when you thrive, innovation thrives.

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; and performing medical device process validation, including installation, operational & performance qualification, in alignment with ISO 13485 standards. Mail resume to Gentherm Medical, LLC, Attn: A. Wylonis, 28875 Cabot Dr, Novi, MI 48377 or email resume to [email protected] Ref 520051

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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; and performing medical device process validation, including installation, operational & performance qualification, in alignment with ISO 13485 standards.

PREFERRED QUALIFICATIONS

NICE TO KNOW

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.