Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Apply quality standards to support the development, qualification and manufacturing of products to meet internal and external requirements.</li><li>Apply statistical tools to analyze data, drive acceptance decisions, improve process capability, and support continuous improvement and lean initiatives.</li><li>Lead Measurement System Analysis (MSA) and supporting product acceptance activities.</li><li>Support and collaborate cross-functionally with engineering, operations, regulatory, customers and suppliers to ensure all change related items are adequately assessed, documented and tested as required.</li><li>Create Master Validation Plan, validation protocols and reports (IQ/OQ/PQ), quality design reviews deliverables, risk management plan, ensure sound start-up of new processes and equipment and development of all quality related documentation. </li><li>Lead resolution of nonconformances, complaints, CAPAs, etc. to resolve quality issues for assigned projects.</li><li>Support supplier quality activities such as supplier selection, qualification, documentation, audits, etc. (QA in FM COS would not oversee, may participate).</li><li>Participate in and occasionally lead internal and external audit.</li><li>Provide guidance to technicians ensuring effective daily support for ongoing tasks.</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field. </li><li>3+ years’ experience in Medical Device or a related regulated industry). </li><li>Understanding of statistical methods, process control, internal/external audits, and the use of quality tools such as Design of Experiments (DOE), Failure Mode and Effects Analysis (FMEA), Control Plan, MSA, SPC, as well as GD&amp;T and fixturing. </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. </li><li>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>Familiarity with design control processes to ensure that design/development, validation, and verification processes align with intended use and performance criteria. </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 Ireland Ltd.

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 Engineer II

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Apply quality standards to support the development, qualification and manufacturing of products to meet internal and external requirements.</li><li>Apply statistical tools to analyze data, drive acceptance decisions, improve process capability, and support continuous improvement and lean initiatives.</li><li>Lead Measurement System Analysis (MSA) and supporting product acceptance activities.</li><li>Support and collaborate cross-functionally with engineering, operations, regulatory, customers and suppliers to ensure all change related items are adequately assessed, documented and tested as required.</li><li>Create Master Validation Plan, validation protocols and reports (IQ/OQ/PQ), quality design reviews deliverables, risk management plan, ensure sound start-up of new processes and equipment and development of all quality related documentation. </li><li>Lead resolution of nonconformances, complaints, CAPAs, etc. to resolve quality issues for assigned projects.</li><li>Support supplier quality activities such as supplier selection, qualification, documentation, audits, etc. (QA in FM COS would not oversee, may participate).</li><li>Participate in and occasionally lead internal and external audit.</li><li>Provide guidance to technicians ensuring effective daily support for ongoing tasks.</li></ul><h1>Qualifications:</h1><ul><li>Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field. </li><li>3+ years’ experience in Medical Device or a related regulated industry). </li><li>Understanding of statistical methods, process control, internal/external audits, and the use of quality tools such as Design of Experiments (DOE), Failure Mode and Effects Analysis (FMEA), Control Plan, MSA, SPC, as well as GD&amp;T and fixturing. </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. </li><li>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>Familiarity with design control processes to ensure that design/development, validation, and verification processes align with intended use and performance criteria. </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 Ireland Ltd.

Quality Engineer II

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Freudenberg

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