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!
Processing of deviations, OOX investigations and incidents in QC
Establishing and tracking corrective and preventive measures for continuous improvement of processes
Conducting GAP assessments and deriving/implementing corrective actions
Support of QC in internal and external audits and inspections
Analysis and evaluation of key figures to ensure a targeted reduction of deviations and incidents
Creation of KPIs and continuous trending in deviation, OOX, incident and CAPA management
Degree in chemistry, pharmacy, biology, biotechnology or comparable
At least 1 year of professional experience
Extensive knowledge of the GMP-regulated environment and ISO 9001 and ISO 13485
Experience in the field of production, quality control or quality assurance of sterile pharmaceuticals
High sense of responsibility and reliability
Strong analysis and communication skills
Process and quality orientation as well as affinity for automated processes
Very good written and spoken German skills
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!