Job Summary Subject Matter Expert (SME) – Laboratory Informatics & LIMS- Remote Experience: 10–15+ Years Role Summary Seeking an experienced Subject Matter Expert (SME) with 15+ years of experience in Life Sciences, Healthcare, Laboratory Informatics, and Clinical Research systems.
Key Responsibilities
- Serve as the primary SME for LIMS and associated laboratory workflows.
- Understand end-to-end clinical laboratory operations including sample lifecycle management, study management, test management, results processing, reporting, and data delivery.
- Gather, analyze, and document business requirements from laboratory stakeholders and clinical operations teams.
- Support onboarding of new laboratories, regions, studies, and customers.
- Collaborate with business stakeholders, laboratory teams, technology teams, vendors, and leadership to define and deliver business solutions.
- Analyze laboratory workflows and translate business requirements into scalable, compliant system solutions.
- Manage risks, dependencies, issues, and mitigation plans to ensure predictable delivery outcomes.
- Oversee data migration, system integration, release planning, change management, and deployment activities.
- Ensure compliance with GxP, GAMP 5, 21 CFR Part 11, data integrity, and validation requirements.
- Support validation activities including URS, FRS, IQ/OQ/PQ, traceability, audit readiness, CAPA, and change control processes.
- Drive continuous improvement, process optimization, and adoption of industry best practices.
Required Skills & Experience
- 10+ years of experience delivering Life Sciences and Healthcare IT programs.
- Strong expertise in:
- Laboratory Information Management Systems (LIMS).
- Chromatography Data Systems (CDS).
- Clinical Trial Management Systems (CTMS/TMS).
- Laboratory Informatics Platforms.
- Clinical and Laboratory Operations.
- Hands-on experience with system implementation, migration, upgrades, integrations, and support.
- Strong understanding of laboratory workflows, sample lifecycle management, study management, and data management.
- Experience with validation and compliance frameworks including GxP, GAMP 5, CSV/CSA, and 21 CFR Part 11.
- Knowledge of data migration, ETL processes, APIs, system integrations, and reporting solutions.
- Strong stakeholder management, business analysis, and consulting skills.
- Experience working in global delivery and regulated environments.
Preferred Qualifications
- Experience across pharmaceutical, biotechnology, CRO, diagnostics, or healthcare organizations.
- Exposure to cloud-based laboratory platforms, analytics, and AI-enabled solutions.
- PMP, CBAP, Agile/Scrum, or relevant Life Sciences certifications.
- Strong leadership, communication, presentation, and problem-solving skills.
Other Job Details
- Interviews: Video interviews.
- Docs required: ID proof will be required.
- Availability: Candidates able to join immediately are preferred.