Digital Tulip MES Engineer

About the Role

The Digitization Operations team at Avantor is responsible for implementing and maintaining digital solutions that enhance manufacturing operations. As a key member of this team, you will have the opportunity to work on exciting projects, collaborate with talented professionals, and contribute to the company's mission to advance life-changing science.

Avantor's commitment to innovation and customer satisfaction is evident in its investment in digital transformation. The company recognizes the importance of staying ahead of the curve in terms of technology and is dedicated to providing its employees with the tools and resources needed to succeed.

What You Will Do

• Develop and deploy GMP-compliant Tulip apps supporting manufacturing operations, including electronic batch records, batch execution steps, and in-process quality checks
• Configure connectors to integrate Tulip with UNS, ERP, LIMS, historians, SCADA/PLC systems, and other validated platforms
• Create and maintain validation documentation, including URS, FRS, IQ/OQ/PQ, risk assessments, and change controls
• Partner with QA and Validation teams to ensure audit readiness and proper lifecycle management of digital systems
• Develop dashboards to provide real-time visibility into batch progress, quality metrics, and equipment performance
• Provide day-to-day support for Tulip apps, connectors, and edge devices in a validated environment
• Troubleshoot issues related to data integrity, device connectivity, and workflow logic
• Monitor system performance, user adoption, and data quality, driving continuous improvement initiatives
• Maintain version control, documentation, and change management in alignment with GMP expectations
• Train operators, supervisors, QA personnel, and engineers on new Tulip workflows and develop SOPs, training materials, and job aids
• Promote a culture of digital adoption, right-first-time execution, and data-driven decision-making

What We Are Looking For

• Bachelor's degree in a relevant field, such as engineering, computer science, or a related discipline
• 2-5 years of experience with MES software applications, including implementation and deployment
• Demonstrated proficiency and hands-on experience with Tulip, preferably in a GMP-regulated environment
• Strong understanding of GMP regulations, including 21 CFR Part 11, Annex 11, and data integrity (ALCOA+) principles
• Experience with low-code development, workflow logic, and data analytics
• Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
• Strong problem-solving skills, with the ability to troubleshoot complex technical issues
• Experience with validation documentation, including URS, FRS, IQ/OQ/PQ, and risk assessments

Nice to Have

• Experience with other MES software applications, such as UNS, ERP, or LIMS
• Knowledge of IT/OT technologies, including historians, SCADA/PLC systems, and edge devices
• Certification in GMP regulations, such as 21 CFR Part 11 or Annex 11
• Experience with agile development methodologies and version control systems
• Strong understanding of pharmaceutical manufacturing processes and regulatory requirements

Benefits and Perks

• Competitive salary and benefits package
• Opportunities for professional growth and development
• Collaborative and dynamic work environment
• Recognition and reward for outstanding performance
• Comprehensive training and development programs
• Flexible work arrangements, including remote work options
• Access to cutting-edge technology and tools
• Chance to work on exciting projects and contribute to the company's mission to advance life-changing science

• Develop a strong understanding of GMP regulations, including 21 CFR Part 11, Annex 11, and data integrity (ALCOA+) principles, to increase your chances of success in this role.
• Showcase your experience with MES software applications, including implementation and deployment, and highlight your proficiency with Tulip.
• Emphasize your ability to work effectively with cross-functional teams, including QA, Operations, IT/OT, Validation, and corporate digital teams.
• Be prepared to provide examples of your experience with validation documentation, including URS, FRS, IQ/OQ/PQ, and risk assessments.
• Highlight your strong problem-solving skills, with the ability to troubleshoot complex technical issues, and your experience with low-code development, workflow logic, and data analytics.
• Research Avantor's company culture and values, and be prepared to discuss how your skills and experience align with the company's mission to advance life-changing science.
• Prepare to discuss your experience with agile development methodologies and version control systems, and be ready to provide examples of your ability to work in a fast-paced, regulated environment.