Senior IT Technical Analyst I, IT Lab Systems
Beamtherapeutics · Cambridge, MA
About this role
**Senior IT Technical Analyst I, IT Lab Systems** **Company Overview:** Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. The company has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities, anchored by base editing technology. **Position Overview:** Beam Therapeutics is seeking a highly motivated Senior IT Business Analyst to join the IT Lab Systems team. This role is responsible for administration, configuration, enhancement, and support of the LabVantage platform, including the Laboratory Execution System (LES), Scientific Data Management System (SDMS), external instrument/system integrations, and supporting laboratory automation technologies. **Key Responsibilities:** • **Laboratory Systems Administration** – Administer LabVantage LIMS, configure master data, manage user administration and security, support system upgrades and lifecycle management • **Laboratory Execution System (LES)** – Design and maintain electronic laboratory worksheets, collaborate on paper-to-digital process conversion, develop reusable templates • **SDMS and Data Management** – Administer SDMS functionality, manage instrument data collection and archival, ensure data integrity and regulatory compliance • **Instrument Integration and Automation** – Design integrations between laboratory instruments and LabVantage, support communication protocols and automated workflows • **Attachment Handler and Development** – Develop LabVantage configurations, support file-based integrations and custom configurations • **Cloud and Integration Support** – Configure Amazon S3-based integrations, collaborate on secure data transfer processes • **Business Partnership** – Work with QC scientists and stakeholders to identify improvements, gather requirements, provide training • **Compliance and Validation** – Support Computer System Validation activities, ensure GxP compliance and 21 CFR Part 11 adherence **Required Qualifications:** • 5+ years supporting LIMS in pharmaceutical, biotechnology, or regulated laboratory environments • 3+ years hands-on LabVantage administration experience • Experience designing LabVantage LES worksheets and supporting SDMS functionality • Understanding of GMP regulations, data integrity requirements, and computerized system validation • Strong analytical, troubleshooting, and problem-solving skills • Ability to translate laboratory workflows into digital solutions **Compensation:** $140,000 – $185,000 USD
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