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Laboratory Systems Consultant

Propharma
5-8 years
₹12–20 LPA
Remote, India, India
15 June 19, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Laboratory Systems Consultant

Company: ProPharma Group
Location: India (Remote / Hybrid as applicable)
Job ID: JR 9853
Employment Type: Full-Time
Department: Laboratory Informatics / Quality & Compliance / R&D Technology

Job Summary

The Laboratory Systems Consultant is responsible for implementing, validating, and supporting laboratory informatics systems such as ELN (Electronic Laboratory Notebook), LIMS (Laboratory Information Management System), and related GxP-compliant digital platforms. The role focuses on system validation, test execution, requirement gathering, and collaboration with laboratory, IT, and quality teams to ensure compliant and efficient system delivery.

Key Responsibilities

Laboratory System Implementation & Support

  • Support implementation, configuration, and enhancement of laboratory systems (ELN, LIMS, LES/MES, eQMS).

  • Assist in system deployment and adoption across laboratory environments.

  • Support system readiness for production release.

Validation & Testing (CSV Activities)

  • Author User Acceptance Testing (UAT) protocols and validation test scripts.

  • Execute UAT, validation, regression, and system testing activities.

  • Perform unit testing in Agile/Scrum sprint cycles.

  • Document test results, deviations, and remediation actions.

Requirements & Documentation Management

  • Gather and analyze business and laboratory requirements.

  • Translate user needs into clear system specifications.

  • Maintain traceability between:

    • Requirements

    • Test cases

    • Validation deliverables

  • Ensure documentation complies with GxP and regulatory standards.

Quality & Compliance

  • Ensure compliance with Computer System Validation (CSV) requirements.

  • Maintain data integrity and regulatory compliance across systems.

  • Support audit readiness and inspection requirements.

  • Track and manage system defects and resolution workflows.

Cross-Functional Collaboration

  • Work closely with laboratory scientists, IT teams, QA teams, and vendors.

  • Support issue resolution and system troubleshooting.

  • Facilitate communication between business users and technical teams.

Agile Delivery Support

  • Participate in Agile/Scrum development cycles.

  • Support sprint planning, testing, and release validation.

  • Ensure continuous improvement of system delivery processes.

Required Qualifications

Education

  • Bachelor’s Degree in:

    • Biology

    • Chemistry

    • Biochemistry

    • Engineering

    • Computer Science

    • Related Scientific or Technical Discipline

Experience

  • Minimum 5 years of experience in:

    • Pharmaceutical or Biopharmaceutical industry

    • Laboratory informatics systems (ELN, LIMS, LES/MES, eQMS)

    • GxP-regulated environments

  • Experience in:

    • Computer System Validation (CSV)

    • UAT testing and validation documentation

    • Agile/Scrum-based project environments

  • Hands-on laboratory experience preferred.

Technical Skills

  • Laboratory Informatics Systems:

    • ELN (Electronic Laboratory Notebook)

    • LIMS (Laboratory Information Management System)

    • LES / MES

    • eQMS platforms

  • Computer System Validation (CSV)

  • UAT & Validation Testing

  • Test Script Development & Execution

  • Requirement Gathering & Traceability Management

  • GxP Compliance & Data Integrity

  • Agile/Scrum Methodologies

Key Skills

  • Analytical Thinking

  • Documentation & Technical Writing

  • Problem Solving

  • Cross-Functional Communication

  • Attention to Detail

  • System Validation Expertise

  • Regulatory Compliance Understanding

  • Stakeholder Management

Key Contribution

  • Ensure reliable and compliant laboratory informatics systems.

  • Support digital transformation in pharmaceutical R&D and QC environments.

  • Improve system quality, efficiency, and regulatory readiness.

  • Bridge scientific and IT functions for seamless system integration.

Salary Criteria

Expected Salary: ₹12–20 LPA for candidates with 5–8 years of experience in laboratory informatics, CSV validation, ELN/LIMS systems, and GxP environments; professionals with strong Agile delivery and enterprise system implementation experience may earn ₹20–25+ LPA depending on technical depth and project leadership exposure.