Freudenberg

Quality Manager

Carrick-on-Shannon, Co

Sponsorship not specifiedDetected 1 day ago

Performance ManagementGMPFDA RegulatoryMedical DevicesLeadership

About the role

Working at Freudenberg: We will wow your world!
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.
Participate and support lean/continuous improvement initiatives and safety initiatives.
Working within the people management systems in the Company to develop others (performance management, rewards and selection process)

Degree / Masters Qualified -preferably in Quality Systems, RegulatoryAffairs, Biomedical Engineering or similar
Minimum 3 years management experience
Knowledge and understanding of ISO 14001, ISO 45001 and ISO 50001.
Minimum of 10 years previous experience involved in Quality Systems compliance within the Medical Devices sector
Extensive knowledge and understanding of the ISO 13485, FDA QMSR and GMP regulations
Lead Auditor qualified preferred
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.

Act as the primary contact for customers regarding quality related issues/activities.

This listing is sourced directly from Freudenberg's careers page and normalized into a canonical job model.