Tulip MES and LabVantage Engineers

Info Way Solutions LLC

  • Indianapolis, IN
  • 30+ days ago

    Highlights

    We are seeking a Senior Implementation Engineer – Tulip MES to design, configure, and deploy digital manufacturing solutions across Elanco's pharmaceutical production facilities. The engineer will work closely with manufacturing, quality, IT/OT, and validation teams to deliver compliant, production-ready MES solutions on the shop floor.

    Numbers & Facts

    LocationIndianapolis, IN

    Description

    Job Description – Senior Implementation Engineer (Tulip MES)

    Role Overview

    We are seeking a Senior Implementation Engineer – Tulip MES to design, configure, and deploy digital manufacturing solutions across Elanco's pharmaceutical production facilities.

    This role is responsible for hands-on implementation, integration, and validation of Tulip-based MES applications to enable:

    · Electronic Batch Records (eBR)

    · Real-time production monitoring

    · Digital work instructions

    · Quality and compliance workflows

    The engineer will work closely with manufacturing, quality, IT/OT, and validation teams to deliver compliant, production-ready MES solutions on the shop floor.

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    Key Responsibilities

    1. Tulip MES Development & Configuration

    · Develop and configure Tulip applications to support:

    o Electronic Batch Records (eBR)

    o Weigh & Dispense workflows

    o Equipment setup, cleaning, and line clearance

    o In-process QA checks and sampling workflows

    · Build operator-facing workflows to digitize manufacturing processes

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    2. System Integration

    Configure and implement integrations with:

    o ERP (SAP)

    o LIMS / Lab systems

    o SCADA / PLC / Historians

    o IoT devices and edge systems

    · Develop connectors using:

    o APIs (REST)

    o SQL / Python

    · Ensure reliable and secure data flow across systems

    Integration across MES, ERP, LIMS, and shop-floor systems is a key responsibility in Tulip implementations

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    3. Validation & Compliance

    · Support and execute validation activities:

    o URS / FRS documentation

    o IQ / OQ / PQ execution

    o Test scripts and traceability matrices

    · Ensure compliance with:

    o GMP / GxP standards

    o 21 CFR Part 11 (e-signatures, audit trails)

    o GAMP 5 / CSV processes

    · Maintain audit-ready MES solutions

    Pharma MES implementations must support validation and regulatory compliance frameworks

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    4. Deployment & Production Support

    · Deploy MES applications across environments:

    o DEV → TEST → PRODUCTION

    · Perform:

    o User Acceptance Testing (UAT) support

    o Go-live and hypercare support

    · Troubleshoot:

    o Workflow issues

    o Integration failures

    o Data integrity issues

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    5. Continuous Improvement

    · Monitor and optimize:

    o System performance

    o User adoption

    o Data quality

    · Identify process improvements:

    o Reduce manual steps

    o Improve batch execution efficiency

    · Enhance digital workflows based on plant feedback

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    6. Cross-functional Collaboration

    · Work closely with:

    o Manufacturing operations (shop floor teams)

    o Quality & validation

    o IT / Digital teams

    · Translate business requirements into MES solutions

    · Support change management and process adoption

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    7. Documentation & Training

    · Develop and maintain:

    o SOPs

    o Technical design documents

    o Validation documents

    · Conduct training for:

    o Operators

    o Supervisors

    o QA personnel

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    Required Skills & Experience

    Experience

    · 5–10 years in MES / Manufacturing IT / Digital Manufacturing

    · 3–5 years hands-on experience in MES implementation

    · Experience with:

    o Tulip MES (Must)

    o Other MES packages, LabVantage integrations (nice to have)

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    Technical Skills

    · Tulip Platform:

    o App building (low-code/no-code)

    o Workflow design

    o Dashboard creation

    · Integration:

    o REST APIs

    o SQL / Python

    o Equipment connectivity (PLC/SCADA)

    · Systems:

    o ERP (SAP)

    o LIMS

    o Manufacturing systems

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    Domain Expertise

    · Pharma / Biotech / Animal Health manufacturing

    · Knowledge of:

    o Batch production processes

    o Quality workflows

    o Traceability and compliance systems

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    Compliance Skills

    · GMP / GxP

    · 21 CFR Part 11

    · CSV / GAMP 5 validation lifecycle

    · Data integrity (ALCOA principles)

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    Soft Skills

    · Strong problem-solving and troubleshooting

    · Effective communication with plant and business teams

    · Ability to work in onsite / shop-floor environments

    · Agile / iterative delivery experience

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    Preferred Qualifications

    · Experience with:

    o Multi-site MES deployments

    o Digital manufacturing / Industry 4.0 programs

    · Exposure to:

    o IoT-enabled manufacturing

    o Real-time analytics / dashboards

    · Certifications:

    o MES platforms or Manufacturing IT

    o Cloud platforms (Azure / AWS)

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