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Information Technology • Consulting • Automation
Leads IT project management and user acceptance testing for LabWare LIMS implementations and laboratory systems validation projects. Responsibilities include requirements gathering, vendor coordination, system upgrades, SOP and UAT script development, data migration, SDLC documentation, qualification, deployment, training, and regulatory compliance with FDA, CAP, CLIA, and GMP requirements. Provides strategic direction across IT, scientific, and management teams in pharmaceutical and other regulated laboratory environments.
Information Technology • Consulting • Automation
Develop, configure, test, validate, and document LabWare LIMS solutions in regulated laboratory environments. Analyze business requirements, prepare technical specifications, write and debug code, participate in design reviews, create validation documentation, and collaborate with subject matter experts and technical teams on global implementations.
Information Technology • Consulting • Automation
Lead scientific data architecture for biopharmaceutical client platforms. Develop information models, scalable relational and NoSQL integration strategies, analytics environments, ontologies, and taxonomies. Translate architectures for technical and business audiences, abstract common solutions across client environments, and serve as a subject matter expert and thought leader for scientific data modeling methodologies.
Information Technology • Consulting • Automation
Manage small to medium Empower CDS and laboratory informatics implementations. Coordinate workstreams, stakeholders, resources, schedules, budgets, risks, scope, quality, communications, and change management. The role serves as an escalation point, maintains client relationships, coaches project resources, controls costs, and ensures delivery within regulated corporate methodologies.
