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Digital Tulip Mes Engineer

astek.pl Logo

Astek

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Location:
Poland , Warsaw

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Contract Type:
Employment contract

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Salary:

16000.00 - 18500.00 PLN / Month

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
  • Clear career path
  • Employee benefits package (Multisport, private healthcare, life insurance)
  • Friendly working atmosphere, team-building events, and team-building meetings
  • Referral system

Additional Information:

Job Posted:
May 05, 2026

Employment Type:
Fulltime
Work Type:
Remote work
Job Link Share:

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