MES Consultant (m/w/d)
Remote
We are seeking a skilled PAS-X MES Consultant to support the digital transformation of manufacturing operations in a GMP-regulated environment. The ideal candidate will design, configure, and optimize PAS-X MES solutions—including but not limited to MBRs—ensuring seamless alignment with manufacturing processes, regulatory requirements, and overall project objectives. This role involves translating business and process needs into robust electronic workflows while guiding stakeholders through best practices in MES design and implementation.
⚠️ A valid EU work permit is required.
Key Responsibilties
- Design, configure, and test PAS-X MES functionalities—including MBRs, master data, equipment models, and workflows—using Körber PAS-X tools and templates.
- Translate manufacturing process descriptions, SOPs, and recipes into compliant electronic workflows
- Collaborate closely with process engineers, automation teams, IT, and QA to ensure accurate representation of manufacturing processes within PAS-X.
- Maintain alignment with global MBR design standards, templates, and naming conventions.
- Support process mapping, user requirement specifications (URS), and functional design documentation.
- Participate in FAT/SAT, IQ/OQ, and UAT testing phases as required.
- Troubleshoot recipe-related issues and support continuous improvement initiatives.
- Ensure adherence to GMP, GAMP5, and data integrity principles.
- Provide training and guidance to end users and key stakeholders.
Must-have
- Bachelor’s or Master’s degree in Engineering, Computer Science, Life Sciences, or related field
- 2+ years of hands-on experience in PAS-X MBR design or MES implementation in the pharmaceutical or biotech industry.
- Strong understanding of GMP, 21 CFR Part 11, and electronic batch record principles.
- Practical experience with PAS-X modules (EBR, Master Data, Equipment Management, etc.).
- Experience in recipe modeling, process mapping, and workflow logic.
Nice-to-have
- Familiarity with automation systems (DeltaV, Siemens PCS 7) and data interfaces (OPC, web services) is an advantage.
- Knowledge of ISA-88 standards and manufacturing process design.
- Fluent in English; German is a plus.
Why Join Us
- Contribute to the digitalization of pharmaceutical manufacturing.
- No stupid managers, no stupid tools that have to be used, no rigid working hours.
- No wasted time in business processes, real responsibility and autonomy
- Expand your knowledge of various industries
- Create content that helps our customers in everyday life
- Real responsibility and challenges in a rapidly developing company
Our services
Our offering
Every employee has the chance to see the impact of their work. They can make a real contribution to the success of the company. Throughout the year, various activities are often organized, such as weekly sports events, team-building activities, monthly after-work gatherings, and much more.
Advantages
- Attractive salary
- Bonus package
Sports
- Sponsored Gym membership
IT Equipment
- Apple IT equipment (incl. personal usage)
Regional / International Projects
- Workcation
