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Analyst - Lab Informatics

Thermo Fisher Scientific
Thermo Fisher Scientific
5-8 years
Not Disclosed
10 Dec. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Title: Analyst – Lab Informatics
Location: Remote, India
Job Type: Full-Time
Category: IT, Data & Tech – Laboratory Informatics

Company Overview:
Thermo Fisher Scientific is a global leader in serving science, driving innovation to solve the world’s toughest challenges—from advancing cancer research to ensuring food and water safety. Join our Data Science, Digital, and IT teams to apply your expertise in analytics, programming, and lab informatics, contributing to meaningful outcomes that improve global health and safety.

Role Overview:
We are seeking an Analyst – Lab Informatics to support the deployment, integration, and operation of laboratory informatics platforms such as LIMS, ELN, CDS, and SDMS in regulated environments. This role ensures laboratory data workflows meet compliance standards, operate efficiently, and enable informed decision-making across regulated manufacturing and quality operations.

Key Responsibilities:

System Configuration & Operational Support

  • Serve as system owner/administrator for lab informatics platforms, managing configurations, access control, and master data.

  • Provide user support, troubleshoot issues, and coordinate with IT and vendors for resolution.

  • Monitor system performance, implement enhancements, and maintain dashboards, reports, and queries for operational insights.

System Implementation & Enhancement

  • Lead or participate in system upgrades, module rollouts, and new implementations.

  • Gather business requirements, translate them into functional specifications, and coordinate implementations with IT teams.

  • Conduct functional and user acceptance testing (UAT) and ensure systems are validated in GxP environments.

  • Maintain documentation including process maps, configuration logs, training materials, and change control records.

Compliance, Validation & Audit Readiness

  • Lead validation activities (IQ/OQ/PQ) and ensure systems meet regulatory standards including 21 CFR Part 11, GAMP 5, and ALCOA+ data integrity principles.

  • Support audit readiness by preparing documentation, reviewing records, and participating in inspections.

  • Maintain audit trails, user logs, and change records per quality system procedures.

Collaboration & Training

  • Act as liaison between lab operations, IT, QA, and vendors to ensure system requirements and project objectives are met.

  • Develop user guides, FAQs, training materials, and deliver onboarding sessions for new users.

  • Coordinate user group meetings for feedback, guidelines, and system improvements.

Team Leadership & Mentorship

  • Guide and mentor junior analysts and support staff in maintaining lab information systems.

  • Delegate tasks, monitor progress, and support professional growth.

  • Promote a collaborative, inclusive, and innovation-driven work environment.

Qualifications & Experience:

  • Bachelor’s degree in Life Sciences, Information Systems, Bioinformatics, or related field.

  • 5–8 years of experience with lab informatics systems in pharmaceutical, biotech, or CDMO settings.

  • Hands-on experience with LIMS (LabWare, Sample Manager), ELN (IDBS), CDS (Empower), SDMS, or analytical instrument software.

  • Strong understanding of software development, system validation, and regulatory compliance (GxP, 21 CFR Part 11).

  • Proficiency in data analysis, business process evaluation, use case development, and user story creation.

Skills & Competencies:

  • Solid knowledge of laboratory workflows including sample management, instrument integration, and test documentation.

  • Expertise in GxP principles, computerized system validation (CSV), and electronic records/e-signature compliance.

  • Strong analytical, problem-solving, and technical writing skills.

  • Familiarity with scripting, relational databases, or basic SQL is a plus.

  • Experience in system integration with enterprise software (SAP, MES, QMS) preferred.

  • Project management and stakeholder collaboration skills, including leading system implementations from design to go-live.

Why Join Thermo Fisher Scientific:

  • Contribute to the modernization of lab operations globally and work on impactful, compliance-driven projects.

  • Collaborate with cross-functional teams and advance your career in lab informatics and data management.

  • Thrive in a workplace that values innovation, collaboration, and purpose-driven results.

Equal Opportunity Employer:
Thermo Fisher Scientific is committed to diversity, equity, and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or legally protected status.

Apply Today: Shape the future of laboratory informatics and contribute to a healthier, cleaner, and safer world.