Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Support the development, documentation, and validation of manufacturing processes (e.g., extrusion, molding, assembly) in compliance with ISO standards, country-specific and GMP regulations.</li><li>Collaborate with cross-functional teams and customers to implement engineering initiatives, including standardization, continuous improvement activities, process improvements, and engineering change orders.</li><li>Assist in the design and qualification of tooling, fixtures, and equipment, including generating and executing IQ/OQ/PQ protocols as required.</li><li>Develop and maintain technical documentation such as BOMs, routers, manufacturing procedures, and work instructions.</li><li>Provide day-to-day engineering support on manufacturing processes, including troubleshooting issues as they arise.  </li><li>Analyze test data, perform root cause investigations, and implement corrective actions to resolve quality issues and support CAPA/NCR activities.</li><li>Improve productivity and reduce scrap/reject rates through automation, tool/process improvements, effective training of production personnel and process enhancements.</li><li>Interfaces with customers and suppliers on project matters, mold and fixture design, validation, and product quality issues."</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's degree in Engineering, Chemistry, Biology, or related science/technical field.  </li><li>0-3 years experience in a regulated industry</li><li>Basic understanding of engineering terminology and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.  </li><li>Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.  </li><li>Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971,   Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States)</li><li>Basic understanding of process validation principles and reports, process window/repeatability studies, DOE’s, IQ/OQ/PQ, and how to validate manufacturing processes to ensure consistent product quality and necessary safety protocols.</li><li>Familiarity with product testing and inspection methods to ensure compliance with specifications and standards.</li><li>Ability to maintain technical documentation, including work instructions, standard operating procedures (SOPs), and production records.</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.

Project Engineer I

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Support the development, documentation, and validation of manufacturing processes (e.g., extrusion, molding, assembly) in compliance with ISO standards, country-specific and GMP regulations.</li><li>Collaborate with cross-functional teams and customers to implement engineering initiatives, including standardization, continuous improvement activities, process improvements, and engineering change orders.</li><li>Assist in the design and qualification of tooling, fixtures, and equipment, including generating and executing IQ/OQ/PQ protocols as required.</li><li>Develop and maintain technical documentation such as BOMs, routers, manufacturing procedures, and work instructions.</li><li>Provide day-to-day engineering support on manufacturing processes, including troubleshooting issues as they arise.  </li><li>Analyze test data, perform root cause investigations, and implement corrective actions to resolve quality issues and support CAPA/NCR activities.</li><li>Improve productivity and reduce scrap/reject rates through automation, tool/process improvements, effective training of production personnel and process enhancements.</li><li>Interfaces with customers and suppliers on project matters, mold and fixture design, validation, and product quality issues."</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's degree in Engineering, Chemistry, Biology, or related science/technical field.  </li><li>0-3 years experience in a regulated industry</li><li>Basic understanding of engineering terminology and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.  </li><li>Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.  </li><li>Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971,   Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States)</li><li>Basic understanding of process validation principles and reports, process window/repeatability studies, DOE’s, IQ/OQ/PQ, and how to validate manufacturing processes to ensure consistent product quality and necessary safety protocols.</li><li>Familiarity with product testing and inspection methods to ensure compliance with specifications and standards.</li><li>Ability to maintain technical documentation, including work instructions, standard operating procedures (SOPs), and production records.</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

Project Engineer I

About the Job

About the Company

Freudenberg

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