Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1>Responsible for leading, development, and management of effective and compliant quality systems and work closely with various cross functional members of site to ensure all requirements are described and meet the needs of regulations and functional excellence. Serve as Management Representative responsible for representing site to all regulatory bodies including registered notified bodies and ensuring management review activities are conduct per regulations. Manage all client quality systems audits and ensure timely response to any audit concerns. Act as the primary contact for customers regarding quality related issues/activities. Ensure all field complaints are response per regulatory requirements. Participate in strategic planning activities to ensure that all quality related requirements are considered when establishing strategic goals and objectives. Participate in new product/project development to ensure quality requirements are established. Work directly with operating entities to ensure that management controls, product life cycle requirements including risk management, inspections, improve yield and product quality, statistical process control analyses and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications. Ensure that all site quality performance indicators (QPI) metrics presented to the management are in sync with site and global requirements and metrics. Participate and support lean/continuous improvement initiatives and safety initiatives. Ensure the quality activities are planned; resources allocated; priorities established and activities executed to meet goals, Working within the people management systems in the Company to develop others (performance management, rewards and selection process); and Creating an energizing work environment that supports the Company’s high performance culture while ensuring and efficient and flexible organization.<h1>Qualifications:</h1><ul><li>Degree / Masters Qualified –preferably in Quality Systems, RegulatoryAffairs, Biomedical Engineering or similar</li><li>Minimum of 10 years previous experience involved in Quality Systems compliance within the Medical Devices sector</li><li>Minimum 3 years management experience</li><li>Extensive knowledge and understanding of the ISO 13485, FDA QMSR and GMP regulations</li><li>Knowledge and understanding of ISO 14001, ISO 45001 and ISO 50001.</li><li>Lead Auditor qualified preferred</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 Manager

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1>Responsible for leading, development, and management of effective and compliant quality systems and work closely with various cross functional members of site to ensure all requirements are described and meet the needs of regulations and functional excellence. Serve as Management Representative responsible for representing site to all regulatory bodies including registered notified bodies and ensuring management review activities are conduct per regulations. Manage all client quality systems audits and ensure timely response to any audit concerns. Act as the primary contact for customers regarding quality related issues/activities. Ensure all field complaints are response per regulatory requirements. Participate in strategic planning activities to ensure that all quality related requirements are considered when establishing strategic goals and objectives. Participate in new product/project development to ensure quality requirements are established. Work directly with operating entities to ensure that management controls, product life cycle requirements including risk management, inspections, improve yield and product quality, statistical process control analyses and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications. Ensure that all site quality performance indicators (QPI) metrics presented to the management are in sync with site and global requirements and metrics. Participate and support lean/continuous improvement initiatives and safety initiatives. Ensure the quality activities are planned; resources allocated; priorities established and activities executed to meet goals, Working within the people management systems in the Company to develop others (performance management, rewards and selection process); and Creating an energizing work environment that supports the Company’s high performance culture while ensuring and efficient and flexible organization.<h1>Qualifications:</h1><ul><li>Degree / Masters Qualified –preferably in Quality Systems, RegulatoryAffairs, Biomedical Engineering or similar</li><li>Minimum of 10 years previous experience involved in Quality Systems compliance within the Medical Devices sector</li><li>Minimum 3 years management experience</li><li>Extensive knowledge and understanding of the ISO 13485, FDA QMSR and GMP regulations</li><li>Knowledge and understanding of ISO 14001, ISO 45001 and ISO 50001.</li><li>Lead Auditor qualified preferred</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 Manager

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About the Company

Freudenberg

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