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Strong Tier-1 pharma brand but niche LabVantage specialization reduces applicant density.
Requires pharma LIMS domain and regulated GxP experience, limiting cross-industry transferability.
Mandates 8+ years, LabVantage hands-on experience, and GxP/CSV compliance, creating strict filtering.
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Lead design, build, and automation of analytical test methods and master data within LabVantage LIMS to support laboratory workflows and compliance.
Develop and maintain instrument drivers and integrations for direct data capture from laboratory instruments into LIMS, ensuring data integrity and automation.
Collaborate with global teams to implement standardized test methods, ensure GxP compliance, support validation and audits, and enhance digital lab ecosystem performance.
Bachelor’s degree in Computer Science, Instrumentation, Chemical Engineering, Analytical Chemistry, or related field.
Minimum 8 years of experience in laboratory informatics in pharma, biotech, or chemicals industry.
At least 4 years of hands-on experience configuring and deploying LabVantage LIMS Master Data including test methods, specifications, and workflows.
Strong knowledge of GxP, 21 CFR Part 11, ALCOA+ data integrity principles, and experience with LabVantage integration to chromatography and analytical instruments.
Proven technical SME with deep expertise in LabVantage LIMS test method management and custom development in regulated environments.
Experience working across global IT, Quality, and Lab Operations teams to deliver compliance-ready lab automation and data governance solutions.
Demonstrated ability to reduce manual efforts through automation and to connect lab automation initiatives with enterprise digital transformation goals.