Senior Developer - LabWare LIMS Seeking exceptional LabWare expertise that can configure complex code, provide in-depth application guidance and support L4 troubleshooting. - Work closely with Product Owner, Quality Assurance and Business Process Owners to effectively and efficiently implement LIMS projects. - Assist with understanding the business requirements, analyze and suggest technical solution for LIMS projects - Create and review deliverables such as technical specification, design documents for LIMS projects - Integrate instruments with Labware LIMS. - Design and implement interfaces with external applications. - Participate in peer reviews of code for coding standards, best practices, functionality, error handling, etc. - Integrate laboratory instruments with scientific software packages. The requirement is to have experience LabWare technical resources that can configure complex code, provide in depth application guidance and support L4 troubleshooting. - Super user will not fit. The right candidates will need to have deep technical background (LIMS programing, infrastructure, msut have LIMS basic programming language, JavaScript for visual workflow, )
Seeking a highly skilled developer/analyst to support and enhance the NTM (Notification to Managers) system — a custom-built SharePoint application that automates management notifications across pharmaceutical Manufacturing and Quality Operations . The role involves designing, integrating, and maintaining data workflows powered by Biovia Pipeline Pilot (PPL) for enterprise-scale ETL (Extract, Transform, Load) operations. This position requires a blend of technical development , business analysis , and quality systems understanding , ensuring the NTM application remains compliant. Key Responsibilities Design, develop, and maintain the NTM (Notification to Managers) application, a critical enterprise solution for automated alerts and escalation workflows within Pfizer’s Quality and Manufacturing systems. Build and optimize ETL workflows using Biovia Pipeline Pilot , ensuring accurate, validated data aggregation from multiple external systems. Apply Business Analysis and Quality Assurance expertise to define, refine, and validate system requirements that meet Pfizer’s compliance and process needs. Integrate data from multiple enterprise platforms, including LIMS, MES, EMDA, SAP, and Quality Management Systems , enabling a unified and consistent notification framework. Implement business logic and workflow automation for NTM processes, ensuring traceability , timely escalation , and compliance with GxP and audit requirements . Collaborate closely with IT, QA, and Business Process Owners to gather requirements, validate technical solutions, and oversee full lifecycle testing for new features and updates. Develop and maintain comprehensive documentation including URS, FRS, IQ/OQ/PQ , validation reports, and training materials to support system audits and GxP compliance. Technical Environment Technologies: SharePoint, Biovia Pipeline Pilot (PPL), Oracle/SQL Databases, REST APIs Integrations: LIMS, EMDA, MES, SAP, and external data sources Processes Supported: Notification to Management (NTM), Quality Incident Tracking, Escalation Management Ideal Candidate Profile 5+ years of experience in SharePoint application development with exposure to Life Sciences or GxP-regulated environments . Strong experience with ETL tools , particularly Biovia Pipeline Pilot (PPL) . Solid understanding of Quality Systems, NCMR/CAPA , and related Pharma Manufacturing processes . Strong analytical and communication skills with the ability to partner effectively with global stakeholders.