Job Description
Position :
Senior Implementation Engineer Tulip MES Location :
Indianapolis, IN Onsite Duration:
1+ Year Role Overview:
We are seeking a highly skilled Senior Implementation Engineer Tulip MES to design, configure, implement, and support digital manufacturing solutions across pharmaceutical production facilities. The ideal candidate will be responsible for the end-to-end deployment of Tulip-based Manufacturing Execution System (MES) applications, enabling Electronic Batch Records (eBR), real-time production monitoring, digital work instructions, and quality/compliance workflows. This role requires close collaboration with Manufacturing, Quality, Validation, IT/OT, and business stakeholders to deliver compliant, scalable, and production-ready MES solutions. Key Responsibilities:
Tulip MES Development & Configuration Design, develop, and configure Tulip MES applications to support manufacturing operations. Build and deploy solutions for:
Electronic Batch Records (eBR) Weigh & Dispense processes Equipment setup, cleaning, and line clearance workflows In-process quality checks and sampling activities Develop operator-centric digital workflows to streamline and standardize manufacturing processes. Create dashboards, forms, and workflow automation using the Tulip platform. System Integration Design and implement integrations between Tulip MES and enterprise/shop-floor systems, including: SAP ERP LIMS and laboratory systems SCADA, PLCs, and process historians IoT devices and edge computing platforms Develop and configure integrations using: REST APIs SQL Python Ensure secure, reliable, and compliant data exchange across manufacturing systems. Support connectivity between MES, ERP, LIMS, and production equipment. Validation & Compliance Support computer system validation (CSV) activities throughout the project lifecycle. Develop and maintain validation documentation, including: User Requirement Specifications (URS) Functional Requirement Specifications (FRS) IQ/OQ/PQ
protocols and execution Test scripts and traceability matrices Ensure MES solutions comply with: GMP and GxP requirements FDA 21 CFR
Part 11 regulations GAMP 5 validation guidelines Maintain audit-ready systems and support regulatory inspections. Deployment & Production Support Manage application deployments across Development, Test, and Production environments. Support User Acceptance Testing (UAT), go-live activities, and post-production hypercare. Troubleshoot and resolve:
Workflow and application issues Integration failures Data integrity and system performance issues Provide ongoing support for MES applications and production users. Continuous Improvement Monitor system performance, user adoption, and data quality metrics. Identify opportunities to:
Eliminate manual processes Improve manufacturing efficiency Enhance batch execution performance Implement process improvements and optimize digital workflows based on business feedback. Cross-Functional Collaboration Partner with Manufacturing Operations, Quality Assurance, Validation, and IT teams to understand business requirements. Translate operational needs into scalable MES solutions. Support change management initiatives and drive user adoption of digital manufacturing technologies. Participate in project planning, workshops, and stakeholder meetings. Documentation & Training Create and maintain: Standard Operating Procedures (SOPs) Technical design documentation Validation and compliance documentation User guides and training materials Conduct training sessions for operators, supervisors, QA personnel, and business users. Required Skills & Experience:
Experience 5 10 years of experience in MES, Manufacturing IT, or Digital Manufacturing environments. 3 5 years of hands-on experience implementing MES solutions. Proven experience with Tulip MES platform implementations. Experience integrating MES with ERP, LIMS, and manufacturing systems. Exposure to LabVantage integrations and other MES platforms is preferred. Technical Skills Strong expertise in Tulip platform development, including: Application configuration and development Workflow design and automation Dashboard and analytics creation Experience with: REST APIs SQL Python scripting PLC/SCADA
connectivity Knowledge of enterprise and manufacturing systems including SAP, LIMS, and production applications. Domain Expertise Experience in Pharmaceutical, Biotechnology, Life Sciences, or Animal Health manufacturing environments. Strong understanding of:
Batch manufacturing processes Quality management workflows Traceability and compliance requirements Compliance & Validation Working knowledge of: GMP and GxP regulations FDA 21 CFR
Part 11 Computer System Validation (CSV) GAMP 5 framework ALCOA data integrity principles Soft Skills:
Excellent analytical and troubleshooting abilities. Strong communication and stakeholder management skills. Ability to work effectively in manufacturing and shop-floor environments. Experience working in Agile and iterative project delivery environments. Preferred Qualifications:
Experience supporting multi-site MES implementations. Exposure to Industry 4.0 and Digital Manufacturing transformation initiatives. Knowledge of IoT-enabled manufacturing environments. Experience with real-time analytics, reporting, and operational dashboards. Relevant certifications in:
MES platforms Manufacturing IT systems Cloud technologies (Azure, AWS) Experience working within regulated pharmaceutical manufacturing environments. Thanks & Regards, Vijay Yadav Global Applications Solution US :
+1 | India:
+91 9898 277 587 Email:
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