For more than 20 years, our production, development and logistics site in Friedberg has been one of the most important locations in the world.
Whether you are starting your career or experienced in your profession – we offer you the right start. Contribute yourself and your ideas and become part of our team!
Handle incidents and deviations in production according to valid requirements
Performing root cause analyses as part of incident and deviation processing
Developing, establishing and tracking corrective and preventive measures for the continuous improvement of PU Friedberg's processes
Support of continuous improvement processes with a focus on increasing product quality, compliance and efficiency
Audit support
Degree in chemistry, pharmacy, biology, biotechnology or comparable
At least 3 years of professional experience in a comparable environment desirable
Knowledge of the EU-GMP & FDA regulated environment as well as ISO 9001 and ISO 13485 would be an advantage
Experience in the field of manufacturing, quality control or quality assurance of sterile medicines desirable
Experience with root cause analysis techniques is an advantage
High sense of responsibility and reliability
Strong analytical and evaluation skills
Communication and cooperation skills as well as process and quality orientation
Very good knowledge of German and good written and spoken English
We offer you an exciting working environment and a position that can be the starting point for further development in our company, as well as the opportunity to make a valuable contribution to improving the quality of life of sick people around the world with us. We are a company bound by collective bargaining agreements with numerous benefits such as employer-financed pension schemes and accident insurance, free employee parking, employee discount programs, a canteen with meal allowance, an occupational health service and many other benefits!
Shape the future together with us – become part of #futurefresenius and apply now via our online portal!