Job Description

Job Description

  •  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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