About the Role: We are seeking a highly skilled ETL Developer to join our EMDA (Environmental Monitoring Data Analytics) team. The role focuses on developing, deploying, and maintaining ETL workflows for a GMP-validated platform used across Pfizer’s global manufacturing sites. The candidate will work with Biovia Pipeline Pilot, integrating data from multiple sources, ensuring high-quality data analytics, and supporting environmental monitoring initiatives. Key Responsibilities: Design, develop, and optimize ETL protocols using Biovia Pipeline Pilot v2017R2 to extract, transform, and load data from lab systems (gLIMS, MODA, LabWare, Thermo Fisher) and flat files (Excel, CSV). Configure and maintain ETL parameters including target DB environments (Dev, Test, Stage, Prod), data classes, study identifiers, folder paths, and runtime settings. Integrate and transform data into the Oracle 19c business layer , ensuring data quality and compliance with GMP standards. Troubleshoot ETL failures, protocol errors, ODBC connectivity issues, and Oracle-specific exceptions. Collaborate with DBAs and EMDA support teams to resolve data access, performance, and integration issues. Support audit trail retrieval , data verification processes, and validation documentation (ADLC plans, SOPs, design specifications). Participate in Agile development cycles and contribute to continuous improvement initiatives. Interpret environmental monitoring data and support EMDA modules including: Heatmaps MODA History & Trend Check Utility/Water Trending Automated Reports ASRAT (Aseptic Site Risk Assessment Tool) Skills & Qualifications: Strong experience with Biovia Pipeline Pilot and ETL workflow design. Proficient in Oracle 19c, SQL Server , and working with flat file data sources. Experience with lab systems integration (gLIMS, MODA, LabWare, Thermo Fisher). Strong troubleshooting skills for ETL and database-related issues. Knowledge of GMP regulations , environmental monitoring data, and validation documentation. Agile development experience and collaborative mindset. Preferred Experience: Prior experience in pharmaceutical or biotech environments . Hands-on experience with EMDA modules and data visualization tools.
About the Role We are seeking a highly skilled Senior LabWare LIMS Developer with deep technical expertise in LabWare V8 to join our QC Labs team. This is not a super-user role we are looking for a technical expert who can configure complex code, integrate lab instruments, and provide Level 4 troubleshooting and guidance. The ideal candidate will collaborate with Product Owners, QA teams, and Business Process Owners to implement and support end-to-end LIMS solutions . Key Responsibilities Configure and customize LabWare LIMS workflows using LabWare scripting and JavaScript . Integrate laboratory instruments and scientific software packages with LabWare LIMS. Design and implement interfaces with external applications. Analyze business requirements and recommend technical solutions for LIMS projects. Create and review technical specifications, design documents, and code deliverables. Participate in peer code reviews , ensuring best practices, error handling, and system performance. Provide L4 technical support for complex system issues. Collaborate with cross-functional teams to deliver LIMS projects efficiently. Required Skills & Experience 610+ years of overall experience in LIMS or related laboratory systems. 46+ years of hands-on experience in LabWare LIMS development (V8) . Strong LabWare scripting and JavaScript skills for workflow customization. Experience with instrument and application integration . Proven track record in Level 4 troubleshooting and complex technical issue resolution. Ability to analyze business requirements and translate them into technical solutions . Experience in writing technical specifications, design documents, and participating in code reviews. Strong communication skills and ability to collaborate with global teams. Preferred Experience in Pharmaceutical, Biotechnology, or Life Sciences QC labs . Familiarity with Regulatory compliance and validation processes . Why Join Us Work on cutting-edge LIMS projects supporting global QC operations. Collaborate with a highly skilled, cross-functional team . Opportunities for professional growth and technical leadership .