Description

We have a clear commitment: putting best-possible solutions in the hands of medical professionals, enabling them to find the right answer to the challenge they face. Fresenius Kabi is a driver of healthcare for the coming decade. We truly live diversity and value different backgrounds and motivations. Around the world, all of us are committed to our shared endeavor: caring for life.

#careerswithapurpose at Fresenius

Over 300,000 people across the globe work at Fresenius to provide better ever medicine for ever more people. Our independent business segments Fresenius Medical Care, Fresenius Kabi, Fresenius Helios and Fresenius Vamed offer a wide spectrum of products and services in the health sector. We offer you the opportunity to make a difference with your career – and to become part of our impressive growth story.

As a Manager MES Pharma (m/w/d), you will contribute your expertise to the digitization of our production sites as part of our globally operating department, thereby actively helping to improve the time-to-market of our internal customers. In doing so, you will benefit from our broad expert knowledge and our global network as one of the world’s leading companies in the areas of nutrition, infusion, pharmaceuticals and medical devices. Fresenius Kabi employees work in a culture that is characterized by a collaborative and modern environment with many opportunities for personal development and emphasizes team spirit as well as customer satisfaction.

  • Lead the MES Pharma team and take responsibility for the implementation and optimization of the Manufacturing Execution System (MES) within a pharmaceutical environment.
  • Strategically plan and manage all projects related to our MES Pharma Solutions, including deployment, customization, and maintenance of the software.
  • Collaborate with internal stakeholders (production, quality assurance, IT) and external partners to ensure seamless integration of the MES into existing processes and systems.
  • Analyze and improve existing workflows to enhance efficiency, quality, and compliance in line with GMP regulations.
  • Ensure adherence to regulatory requirements, particularly in the pharmaceutical industry (e.g., GxP, FDA 21 CFR Part 11).
  • Develop and implement KPIs to measure success and drive continuous improvement of the system.

  • A degree in computer science, engineering, biotechnology, pharmacy, or a related field.
  • Several years of professional experience in managing MES implementation projects, preferably in the pharmaceutical or regulated industry.
  • In-depth knowledge of PAS-X or similar MES platforms.
  • Proven leadership experience, with the ability to develop and motivate teams.
  • Strong understanding of relevant regulatory requirements (GMP, GxP, FDA, EU Annex 11).
  • Excellent analytical and organizational skills with a solution-oriented mindset.
  • Outstanding communication and presentation skills in English (German language skills are an advantage).
  • Willingness to travel (max. 30%)