With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
We are currently looking for an experienced Quality Management Engineer, Supplier Auditor to join our Quality department in Feldkirchen, Germany, part of the product area Critical Care at Getinge. This role will support the organization as Supplier Auditor, will closely collaborate with our R&D department to assist with their projects, will work on our CSV process, and conitonously improve our quality management system.
Quality Management Engineer, Supplier Auditor (m/f/d)
Responsible for the annual supplier audit schedule
Planning, preparation and auditing suppliers as Lead Auditor
Participation in the selcetion, evaluation, monitoring and development of suppliers
Cooperation with suppliers on quality related topics (e.g., in case of external audits)
Support in the CSV process from quality perspective
Assistance with the Design Change Control and Design Control process
Performance of internal audits (Internal Auditor)
Preparation and support of external audits (notified bodies, authorities, customers)
Continous contribution on process improvement and aligment with other Critical Care site
Provision and reporting of monthly KPIs
Maintenance, review and approval of QMS related documentation and record
Collaboration in internal quality projects
Degree in medical technology, engineering, science or similar relevant education
Minimum 3 years of hands-on expierence in Quality and Environmental Management ISO13485
At least 2 year experience as Lead Auditor in supplier audits
Background in close collaboration with R&D projects and CSV processes
Relevant knowledge for implementation and usage of applicable standars and regulations
Proven external and/or internal trainings in QM / ISO13485 / FDA / EU MDR
Ideally trained as an Internal Auditor
Demonstrated history in Quality/ Environmental related projectes (e.g., CAPAs, EU MDR uplift) are an advantage
Written and spoken fluency in English and German
On-site work for at least 1-2 days per week is expected; readiness to travel (25%)
High quality products in a life-saving environment
Attractive conditions, 30 paid vacation days per year
Possibility of mobile working
Modern workplace equipment
Business Bike and corporate benefits
Career opportunities in a well-known company
Individual trainings