Consultant Pharma MES involved in MES systems projects for pharmaceuticals. Responsibilities include project implementation, configuration, and process analysis in a regulated environment.
Responsibilities
Active participation in projects for the implementation and further development of MES systems
Independent configuration and implementation of MES solutions across pharmaceutical manufacturing processes
Creation and maintenance of electronic batch records (EBR) in the MES
Process analysis in a regulated GxP environment and identification of optimization opportunities
Support for testing, validation activities (CSV) and go-live phases
Requirements
At least two years of professional experience in consulting, industry, or in the context of MES projects
Solid knowledge of Rockwell PharmaSuite MES
Experience with recipe management, particularly working with electronic batch records (EBR)
Good understanding of pharmaceutical manufacturing processes in a regulated GxP environment
Very good German and good English skills
Benefits
Exciting projects
Diverse development opportunities
Flexible working environment with fair compensation and opportunities for training and professional development
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