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Digital Tulip MES Engineer

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Astek

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Location:
Poland , Warsaw

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Category:
IT - Software Development

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Contract Type:
Not provided

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Salary:

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Job Description:

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 – being a member of the Competence Center community from day one is an opportunity to develop your skills, participate in various conferences, and share knowledge and experience with people who face the same challenges every day
  • Clear career path
  • Employee benefits package (Multisport, private healthcare, life insurance)
  • Friendly working atmosphere, team-building events, and team-building meetings
  • Referral system with bonus up to 7,000 PLN

Additional Information:

Job Posted:
May 05, 2026

Employment Type:
Fulltime
Work Type:
Remote work
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