Completed university degree in engineering or natural sciences, pharmacy or comparable qualification
Several years of professional experience (at least 3-5 years) in the GMP-regulated environment of the pharmaceutical industry, ideally in Quality Assurance or Validation
Solid experience in Computer System Validation (CSV) – demonstrably proven through completed validation projects
Practical knowledge in the area of data integrity and GAMP 5
Experience with LIMS (Laboratory Information Management Systems) or comparable GxP-relevant IT systems is an advantage.
Experience with Laboratory Execution Systems (LES) is a valuable asset for potential future project phases.
Project experience in interdisciplinary, international teams – ideally in implementation or migration projects
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