Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Execute project tasks and/or lead low complexity projects under close supervision.</li><li>Create/maintain Design Controls documentation in accordance with established regulatory requirements and SOPs.</li><li>Translate User Needs into Design Input Requirements to comply with regulatory requirements and best-practice standards. Perform testing to verify the design input requirements.</li><li>Generate CAD models &amp; drawings based on theoretical concepts.</li><li>Build and test prototype devices.</li><li>Identify suppliers in the context of product development activities.</li><li>Coordinate testing with internal or external partners, including Design Validation to ensure devices meet user needs.</li><li>Facilitate project team meetings.</li><li>Select materials for prototypes and finished medical devices.</li><li>Lead or assist in creating technical document, such as protocols and reports.</li></ul><h1>Qualifications:</h1><ul><li>0-2 years of Medical Device design &amp; development experience.</li><li>Bachelor of Science in Mechanical, Biomedical Engineering, or related discipline. Master’s degree preferred.</li><li>21CFR Part 820.30 Design Controls, ISO 13485, ISO 14971 ISO 10993 and IEC 62366.</li><li>3D solid modelling (e.g. SolidWorks or related software).</li><li>Hands-on experience with machining and 3D prototyping methods preferred.</li><li>Knowledge of silicone and plastic molding preferred.</li><li>Good communication &amp; interpersonal skills.</li><li>Good mechanical, analytical &amp; problem-solving skills.</li><li>Willingness to learn and develop new skills.</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.

Product Development Engineer I

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Execute project tasks and/or lead low complexity projects under close supervision.</li><li>Create/maintain Design Controls documentation in accordance with established regulatory requirements and SOPs.</li><li>Translate User Needs into Design Input Requirements to comply with regulatory requirements and best-practice standards. Perform testing to verify the design input requirements.</li><li>Generate CAD models &amp; drawings based on theoretical concepts.</li><li>Build and test prototype devices.</li><li>Identify suppliers in the context of product development activities.</li><li>Coordinate testing with internal or external partners, including Design Validation to ensure devices meet user needs.</li><li>Facilitate project team meetings.</li><li>Select materials for prototypes and finished medical devices.</li><li>Lead or assist in creating technical document, such as protocols and reports.</li></ul><h1>Qualifications:</h1><ul><li>0-2 years of Medical Device design &amp; development experience.</li><li>Bachelor of Science in Mechanical, Biomedical Engineering, or related discipline. Master’s degree preferred.</li><li>21CFR Part 820.30 Design Controls, ISO 13485, ISO 14971 ISO 10993 and IEC 62366.</li><li>3D solid modelling (e.g. SolidWorks or related software).</li><li>Hands-on experience with machining and 3D prototyping methods preferred.</li><li>Knowledge of silicone and plastic molding preferred.</li><li>Good communication &amp; interpersonal skills.</li><li>Good mechanical, analytical &amp; problem-solving skills.</li><li>Willingness to learn and develop new skills.</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

Product Development Engineer I

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About the Company

Freudenberg

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