Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>You contribute to the further development of Regulatory Affairs and quality management systems in accordance with MDR and ISO 13485</li><li>You coordinate international approval and registration procedures for medical devices containing medicinal components</li><li>You prepare and maintain technical documentation and communicate with customers, suppliers, and authorities worldwide</li><li>You handle regulatory authority inquiries and research country-specific approval requirements</li><li>You support R&amp;D, production, and logistics in matters of regulatory compliance and quality</li><li>You maintain change management processes and support design and process changes</li><li>You prepare and conduct audits, including communication with customers and authorities</li></ul><h1>Qualifications:</h1><ul><li>You hold a degree in natural sciences, biomedical engineering, or a comparable qualification</li><li>You have experience in the medical device industry, ideally also in the validation of sterilization processes (ETO)</li><li>You are familiar with regulatory requirements for medical devices in the EU (EU MDR, ISO standards, MPDG); knowledge of pharmaceutical regulations (AMG, GMP) and international standards (US FDA) is an advantage</li><li>You have a good understanding of medical devices and functional pharmaceutical coatings</li><li>You work independently, in a structured manner, and as part of a team</li><li>You are proficient in MS Office, Adobe Acrobat, and quality management systems according to EN ISO 13485</li><li>You have excellent written and spoken German and English 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.Hemoteq AG

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.

Manager Regulatory Affairs (w/m/d)

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>You contribute to the further development of Regulatory Affairs and quality management systems in accordance with MDR and ISO 13485</li><li>You coordinate international approval and registration procedures for medical devices containing medicinal components</li><li>You prepare and maintain technical documentation and communicate with customers, suppliers, and authorities worldwide</li><li>You handle regulatory authority inquiries and research country-specific approval requirements</li><li>You support R&amp;D, production, and logistics in matters of regulatory compliance and quality</li><li>You maintain change management processes and support design and process changes</li><li>You prepare and conduct audits, including communication with customers and authorities</li></ul><h1>Qualifications:</h1><ul><li>You hold a degree in natural sciences, biomedical engineering, or a comparable qualification</li><li>You have experience in the medical device industry, ideally also in the validation of sterilization processes (ETO)</li><li>You are familiar with regulatory requirements for medical devices in the EU (EU MDR, ISO standards, MPDG); knowledge of pharmaceutical regulations (AMG, GMP) and international standards (US FDA) is an advantage</li><li>You have a good understanding of medical devices and functional pharmaceutical coatings</li><li>You work independently, in a structured manner, and as part of a team</li><li>You are proficient in MS Office, Adobe Acrobat, and quality management systems according to EN ISO 13485</li><li>You have excellent written and spoken German and English 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.Hemoteq AG

Manager Regulatory Affairs (w/m/d)

About the Job

About the Company

Freudenberg

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