About this role
Role Overview
- Designing, deploying, and sustaining Tulip applications within a GMP‑regulated pharmaceutical manufacturing environment
- Build and deploy GMP‑compliant Tulip apps supporting manufacturing operations
- Ensure all Tulip applications comply with GMP, GAMP 5, 21 CFR Part 11, Annex 11, and data integrity principles
- Provide day‑to‑day support for Tulip apps, connectors, and edge devices in a validated environment
- Train operators, supervisors, QA personnel, and engineers on new Tulip workflows
- Partner with QA and Validation teams to ensure audit readiness
Requirements
- Bachelor’s degree and/or equivalent experience
- 2–5 years of experience with MES software applications
- Demonstrated proficiency and hands-on experience with Tulip strongly preferred
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Professional development opportunities