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We are currently looking for a candidate for the position of Digital Tulip MES Engineer (he/she) for our client – global digital transformation solutions provider.
Job Responsibility:
Develop and deploy GMP-compliant Tulip applications for electronic batch records (EBR), quality workflows, material traceability, CAPA processes, and audit trails
Configure and integrate Tulip applications with ERP, LIMS, SCADA/PLC systems, historians, and other validated manufacturing platforms
Create dashboards providing real-time visibility into production progress, quality metrics, and equipment performance
Ensure compliance with GMP, GAMP 5, 21 CFR Part 11, Annex 11, and ALCOA+ data integrity principles
Prepare and maintain validation documentation, including URS, FRS, IQ/OQ/PQ protocols, risk assessments, and change controls
Collaborate with QA, Validation, and IT/OT teams to ensure audit readiness and proper lifecycle management of digital systems
Provide ongoing support for Tulip applications, troubleshoot issues related to data integrity, device connectivity, and workflow logic
Monitor system performance and data quality while driving continuous improvement initiatives
Maintain documentation, version control, and change management processes in line with GMP requirements
Train operators, engineers, and QA personnel on new workflows and prepare SOPs and training materials
Partner with process engineering and operations teams to implement digital solutions in new processes and capital projects
Requirements:
Have a bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related field
Have 2–5 years of experience in pharmaceutical manufacturing, process engineering, or digital systems
Have hands-on experience with Tulip or similar low-code MES and digital work instruction platforms
Understand GMP, GAMP 5, 21 CFR Part 11, Annex 11, and data integrity requirements
Have experience validating computerized systems in regulated environments
Have knowledge of SQL, APIs, OPC UA, or IoT integrations
Have experience with Lean, Six Sigma, or operational excellence methodologies
Are familiar with pharmaceutical systems such as ERP, LIMS, MES, SCADA, and PLCs
Have strong analytical and problem-solving skills with the ability to translate GMP workflows into digital solutions
What we offer:
Long-term collaboration
Technical training, certifications, and skills development
Competence Center mentoring
Clear career path
Employee benefits package (Multisport, private healthcare, life insurance)
Friendly working atmosphere, team-building events, and team-building meetings