MES Consultant (m/f/d)

MES Consultant (m/w/d) for the location Starnberg (Percha), Münster or Regensburg Would you like to make a valuable contribution to the health of patients? And do you have something really meaningful? Then we look forward to seeing you! Excellence beyond manufacturing – we stand as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 locations. Our location in Starnberg is the headquarters of Aenova Group.

Analysis and design of production processes including MBR design, including request recording, Fit-to-Standard evaluation, modelling of Master Batch Records and configuration of relevant parameters. Ensuring smooth system integration, in particular by connecting to ERP systems, as well as the integration of shopfloor machines and equipment. Implementation of a structured release management in the SaaS environment, including evaluation of regular updates and patches as well as analysis of the release notes regarding possible effects. Providing support and training, in particular in 2nd level support with error analysis and troubleshooting as well as performing trainings for key users. Further development of the system landscape and production processes, by identifying optimization potentials, as well as configuration and development of reports and dashboards for evaluating production characteristics.

Comprehensive expertise in the MES environment with deep knowledge in PAS‐X, in particular in the design of Master Batch Records, the workflow configuration and the safe application of GMP guidelines and CSV requirements. Secure understanding of system integration between MES, ERP systems (SAP) and automation levels, including interfaces to LIMS and SCADA systems, as well as the ability to analytically capture complex pharmaceutical manufacturing processes and transfer them to digital processes. Finded understanding of pharmaceutical order production, combined with flexibility and resilience to respond to changing priorities in the dynamic CDMO environment. Multiannual professional experience (at least 3-5 years) in the pharmaceutical industry, biotechnology or a comparable regulated environment, supplemented by pronounced communication and presentation strength. Very good knowledge of German and English in word and writing to convey technical content clearly and to communicate safely with international stakeholders.

Are you looking for new challenges in a competitive environment? And you want to create them creatively and independently? Do you prefer a “get-it-done” culture and think in solutions rather than in problems? What are you waiting for? We would like to explain our corporate benefits in a personal conversation! !