Senior IT Business Analyst I – Lab Systems

Compliance Group Inc

Cambridge (MA)

On-site

USD 110,000 - 140,000

Full time

47 hours ago
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Job summary

Compliance Group Inc. seeks a Senior IT Business Analyst I to support and enhance laboratory systems, focusing on LabVantage LIMS, LES, and SDMS. You will administer, configure, and maintain these systems while collaborating with QC, QA, IT, and lab teams.

Responsibilities include developing lab worksheets and workflows, enabling instrument integrations, managing data exchanges, and ensuring GxP compliance and data integrity in a GMP environment.

Qualifications

  • 5+ years of LIMS experience in Pharma/Biotech.
  • 3+ years of hands-on LabVantage administration.
  • Experience with LabVantage LES and SDMS.
  • Laboratory instrument integration and file-based data exchange experience.
  • Knowledge of GMP, CSV, GAMP 5, ALCOA+, and 21 CFR Part 11.

Responsibilities

  • Administer, configure, and maintain LabVantage LIMS, LES, and SDMS.
  • Develop and maintain electronic laboratory worksheets and workflows.
  • Support laboratory instrument integrations and automation.
  • Manage data exchange, file-based integrations, and AWS S3.
  • Partner with QC, QA, IT, and laboratory teams.
  • Support CSV, GxP compliance, data integrity, and 21 CFR Part 11 requirements.

Skills

LIMS experience
Regulatory compliance
Data integration
Cross-functional collaboration

Tools

LabVantage LIMS
LabVantage LES
LabVantage SDMS
AWS S3

Job description

Client is seeking an experienced Senior IT Business Analyst I to support and enhance laboratory systems, primarily LabVantage LIMS, LES, and SDMS.

Key Responsibilities:
  • Administer, configure, and maintain LabVantage LIMS, LES, and SDMS.
  • Develop and maintain electronic laboratory worksheets and workflows.
  • Support laboratory instrument integrations and automation.
  • Manage data exchange, file-based integrations, and AWS S3.
  • Partner with QC, QA, IT, and laboratory teams.
  • Support CSV, GxP compliance, data integrity, and 21 CFR Part 11 requirements.
Required Qualifications:
  • 5+ years of LIMS experience in Pharma/Biotech.
  • 3+ years of hands-on LabVantage administration.
  • Experience with LabVantage LES and SDMS.
  • Laboratory instrument integration and file-based data exchange experience.
  • Knowledge of GMP, CSV, GAMP 5, ALCOA+, and 21 CFR Part 11.
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