Job Description
<p><p><b>Role Overview : <br/></b><br/>We are looking for a talented Tulip Developer to join our dynamic team, focused on building, deploying, and maintaining applications on the Tulip platform.<br/><br/>The ideal candidate will have extensive experience working in regulated environments, particularly within pharmaceutical manufacturing, ensuring digital manufacturing processes comply with GxP regulations and quality standards.<br/><br/>You will collaborate closely with business stakeholders, process owners, quality assurance, and IT teams to translate operational requirements into scalable and compliant Tulip applications, enabling process automation, data collection, and enhanced operational efficiency.<br/><br/><b>Key Responsibilities : <br/></b><br/>- Design, develop, configure, and deploy custom applications and workflows on the Tulip platform to support manufacturing operations, quality assurance, and digital transformation initiatives.<br/><br/>- Work closely with process owners, quality teams, and business stakeholders to capture and understand requirements, translating them into functional Tulip-based solutions.<br/><br/>- Develop applications adhering to GxP compliance guidelines including GMP and 21 CFR Part 11.<br/><br/>- Participate actively in system validation activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).<br/><br/>- Integrate Tulip applications with other enterprise systems such as Manufacturing Execution Systems (MES), Enterprise Resource Planning (ERP), Laboratory Information Management Systems (LIMS), SQL databases, and IoT devices to enable seamless data exchange and workflow automation.<br/><br/>- Create and maintain dashboards, custom reports, and analytics within the Tulip platform to support operational monitoring, decision-making, and continuous improvement.<br/><br/>- Provide ongoing support, troubleshoot issues, and implement enhancements to optimize application performance, usability, and reliability.<br/><br/>- Prepare and maintain detailed documentation including functional specifications, validation protocols, test scripts, and change control records in compliance with regulatory standards.<br/><br/>- Engage effectively with cross-functional teams from IT, Quality, Manufacturing, and Operations to ensure successful project delivery and continuous alignment with business needs.<br/><br/><b>Required Qualifications : </b><br/><br/><b>Experience : </b><br/><br/>- Minimum 5 years in software/application development.<br/><br/>- 2-3 years of dedicated experience developing on the Tulip platform within a GxP-regulated pharmaceutical or biotech environment.<br/><br/><b>Regulatory Knowledge : </b><br/><br/>- Strong understanding of GxP, GMP, and 21 CFR Part 11 compliance.<br/><br/>- Hands-on experience with validation processes including IQ, OQ, PQ.<br/><br/><b>Technical Skills : </b><br/><br/>- Proficient in Tulip app development including workflow design, triggers, connectors, and analytics.<br/><br/>- Experience integrating Tulip with MES, ERP, LIMS, IoT devices, and databases (SQL).<br/><br/>- Solid understanding of application lifecycle management in regulated environments.<br/><br/><b>Soft Skills : </b><br/><br/>- Strong analytical and problem-solving capabilities.<br/><br/>- Excellent communication skills for effective collaboration across diverse teams.<br/><br/>- Ability to work independently and manage multiple priorities in a fast-paced environment</p><br/></p> (ref:hirist.tech)