Post: Senior Implementation Engineer (Tulip MES)
Location: Remote (US-Based) with occasional travel to Kansas City, MO, Winslow, ME, and Iowa
Position Type: Full-Time / Permanent
Industry: Pharmaceutical / Biotechnology Manufacturing
🔹 Role Overview
We are seeking a Senior Implementation Engineer – Tulip MES to design, configure, and deploy next-generation digital manufacturing solutions across our pharmaceutical production facilities.
This is a remote-first role requiring occasional travel to our key production sites for deployment and collaboration. You will be responsible for the hands-on implementation, integration, and validation of Tulip-based Manufacturing Execution System (MES) applications. Your work will directly enable Electronic Batch Records (eBR), real-time production monitoring, digital work instructions, and strict quality/compliance workflows.
You will collaborate closely with cross-functional teams—including Manufacturing, Quality, IT/OT, and Validation—to deliver compliant, production-ready MES solutions directly to the shop floor.
🔹 Key Responsibilities
1. Tulip MES Development & Configuration
App Development: Design, build, and configure robust Tulip applications to support critical pharmaceutical operations:
Electronic Batch Records (eBR)
Weigh & Dispense workflows
Equipment setup, cleaning, and line clearance
In-process QA checks and sampling workflows
UI/UX Design: Build intuitive, operator-facing workflows that digitize and simplify complex manufacturing processes on the shop floor.
2. System Integration & Connectivity
Cross-Functional Integration: Bridge the gap between the shop floor and enterprise systems. Configure and implement seamless integrations with:
Connector Development: Develop and maintain secure, reliable data connectors using APIs (REST), SQL, and Python.
🔹 Qualifications & Requirements
📌 Travel Note
Candidates must be willing and able to travel occasionally to facility locations in Kansas City, MO, Winslow, ME, and Iowa.
MES Expertise: Proven experience developing, configuring, and deploying solutions within the Tulip Interfaces platform.
Technical Skills: Proficiency with APIs (REST), SQL databases, and Python scripting for system integration.
Industry Experience: Background in pharmaceutical, biotech, or medical device manufacturing is highly preferred.
Compliance Knowledge: Familiarity with GxP, 21 CFR Part 11, and validation protocols in a regulated production environment.
Collaboration: Strong communication skills with the ability to manage remote timelines while building rapport with on-site automation engineers and operators.
kindly share your CV on
+1