We are looking for a highly skilled MES expert to lead the transition from paper-based to fully digitalized manufacturing processes.
Key Responsibilities :
* Analyze, harmonize, and standardize manufacturing process requirements with stakeholders to ensure optimal alignment with MES solutions.
* Translate business and manufacturing requirements into technical specifications that leverage MES out-of-the-box functionalities.
* Ensure compliance with GMP / GxP / CSV standards throughout the implementation process.
* Collaborate closely with MES vendors, IT architects, and manufacturing process owners to ensure seamless system integration.
* Optimize information flow and data models across shop floor and top floor processes.
Key Requirements :
* 10+ years of experience with MES systems and processes, ideally in the pharmaceutical or medical device industries.
* Proven expertise in MES solutions such as Siemens, Tulip, or Rockwell, with strong knowledge of IT / OT integration.
* Strong understanding of manufacturing processes and information flow within MES environments.
* Experience ensuring GMP / GxP compliance in regulated industries.
* Excellent stakeholder management and communication skills with a focus on collaboration and problem-solving.
Benefits :
* Engage in exciting and innovative projects driving digital transformation in manufacturing processes.
* Work in a dynamic and international environment with cross-functional teams and global stakeholders.
* Opportunities to shape state-of-the-art MES solutions and contribute to cutting-edge digitalization initiatives.
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