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Tier-1 brand and metro location increase interest, but highly specialized LIMS/GxP seniority limits candidate pool.
Strong pharma LIMS and CSV/GxP specialization limits cross-industry transferability.
Strict 12+ years, mandatory LabVantage LIMS and CSV/GxP expertise required.
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Lead end-to-end delivery of LabVantage LIMS implementation, upgrades, and integration programs aligned with business goals and regulatory requirements.
Own CSV strategy and standards, review and approve validation documentation, risk assessments, and test protocols to ensure compliance with quality standards.
Champion DevOps automation and AI to accelerate release cycles, improve quality, and maintain operational stability across global environments.
Bachelor's degree in Computer Science, Information Technology, or related field.
12+ years professional software development experience; minimum 6+ years as Technical Project Manager with LabVantage LIMS (v8.5 or higher) in regulated Life Sciences.
Significant pharmaceutical industry experience focusing on Computer Systems Validation (CSV), GxP, GAMP 5, 21 CFR Part 11 compliance.
Strong expertise in LIMS development, system integrations (RESTful APIs, SOAP, middleware like MuleSoft), and stakeholder management across global, cross-functional teams.
Experienced technical leader with deep LabVantage LIMS expertise within GxP-regulated pharmaceutical environments involving complex system validations.
Capable of managing global cross-cultural stakeholder engagements, translating business needs into compliant technical solutions, and coordinating multi-disciplinary teams.
Proficient in driving automation and AI-enabled process improvements to support regulatory compliance and enhance system release efficiency.