Translation of production processes into MBRs and related master data. In doing so, you will take into account the strict procedures specific to the pharmaceutical industry: Quality Standards, current Good Manufacturing Practices, Standard Operating Procedures, Work Instructions
Daily interdepartmental contacts with supervision within production and quality
Occasional international contacts
Leading improvement projects in the context of quality
Active participation in project teams, operational teams and system teams
Responsible for user support for your Master Batch records (including training and guidance), occasionally also after office hours.
Close collaboration with IT and automation
Your profile
Master's degree in a scientific field or equivalent experience
Interest in MES/ERP systems and their interfaces / affinity wit...
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