Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1>Assists in the completion and assembly of regulatory submissions (both international and domestic). Maintains regulatory files including submissions, technical files, etc. Assists in regulatory body, internal &amp; external audits, product recalls, Vigilance and MDR reportability, as necessary. Interfaces with customer service and engineering on customer complaints and complaint investigations. Ensures customer complaints, MDR’s and global vigilance reporting are addressed in a timely manner according to the risk level per company and regulatory standards. Assists customer service and quality team in improving the customer complaint process and procedures. Management of domestic and international standards, directives, regulations, etc. for gap analysis according to the latest revision. Independently handle problems that arise within area of responsibility. Able to assist Freudenberg Medical departments in gathering data or special assignments with limited assistance. Performs in-depth review of regulatory data/information and provide oversight of query resolution and database to Supervisor/Manager. Able to change priorities when directed by Supervisor/Manager.<h1>Qualifications:</h1>n/aThe 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.VistaMed 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.

Regulatory Compliance Engineer

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1>Assists in the completion and assembly of regulatory submissions (both international and domestic). Maintains regulatory files including submissions, technical files, etc. Assists in regulatory body, internal &amp; external audits, product recalls, Vigilance and MDR reportability, as necessary. Interfaces with customer service and engineering on customer complaints and complaint investigations. Ensures customer complaints, MDR’s and global vigilance reporting are addressed in a timely manner according to the risk level per company and regulatory standards. Assists customer service and quality team in improving the customer complaint process and procedures. Management of domestic and international standards, directives, regulations, etc. for gap analysis according to the latest revision. Independently handle problems that arise within area of responsibility. Able to assist Freudenberg Medical departments in gathering data or special assignments with limited assistance. Performs in-depth review of regulatory data/information and provide oversight of query resolution and database to Supervisor/Manager. Able to change priorities when directed by Supervisor/Manager.<h1>Qualifications:</h1>n/aThe 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.VistaMed Ltd.

Regulatory Compliance Engineer

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About the Company

Freudenberg

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