Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Support the validation activities for a new machine on the manufacturing floor.</li><li>Update procedures in our electronic document management system.</li><li>Assist with the validation activities for a new labeling software program.</li><li>Create new documentation and review existing documentation for compliance with regulations and procedures.</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's Degree (in progress or completed).</li><li>High attention to detail.</li><li>Goal oriented.</li><li>Strong interpersonal, oral and written communication skills.</li><li>Some prior experience with writing and executing Engineering reports and studies.</li><li>Some prior experience with coding/programming.</li></ul>The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.Freudenberg Medical LLC

Freudenberg e-Power Systems is one of the world's leading suppliers of emission-neutral energy systems for heavy-duty applications. With its experience and expertise in battery and fuel cell technology, the company offers tailor-made solutions, in particular combined systems, for sustainable and economical e-mobility. With over 800 employees, Freudenberg e-Power Systems supports its customers from application development through to production, commissioning and service.
The company is part of the global Freudenberg Group, which has four business areas: Seals and Vibration Control Technology, Nonwovens and Filtration, Household Products as well as Specialties and Others. In 2022 the Group generated sales of more than 11 billion euros and employed more than 50,000 associates in around 60 countries.

Quality Intern

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Support the validation activities for a new machine on the manufacturing floor.</li><li>Update procedures in our electronic document management system.</li><li>Assist with the validation activities for a new labeling software program.</li><li>Create new documentation and review existing documentation for compliance with regulations and procedures.</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's Degree (in progress or completed).</li><li>High attention to detail.</li><li>Goal oriented.</li><li>Strong interpersonal, oral and written communication skills.</li><li>Some prior experience with writing and executing Engineering reports and studies.</li><li>Some prior experience with coding/programming.</li></ul>The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.Freudenberg Medical LLC

Quality Intern

About the Job

About the Company

Freudenberg

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