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Job Description
Structured overview of role & requirementsAbout This Role
Lead end-to-end delivery of LabVantage LIMS implementation, upgrades, releases, and validation readiness in a GxP-regulated, global environment.
Own creation and maintenance of execution plans aligned with timelines, budgets, and Quality Management System (QMS).
Drive CSV strategy, manage cross-functional stakeholder coordination, and adopt AI and DevOps automation to improve release speed, quality, and operational stability.
Minimum Requirements
Bachelor's degree in Computer Science, Information Technology, or related field.
12+ years professional experience in software development; minimum 6+ years as Technical Project Manager with LabVantage LIMS (v8.5 or higher) in regulated Life Sciences environment.
Significant experience in pharmaceutical industry focusing on Computer Systems Validation (CSV), deep LIMS or MES implementation experience preferred.
Strong knowledge of GxP, GAMP 5, 21 CFR Part 11, LIMS system integrations (RESTful APIs, SOAP, middleware platforms like MuleSoft).
Ideal Candidate Profile
Technical leader with deep LabVantage LIMS expertise and strong quality mindset capable of influencing global stakeholders.
Proven ability managing diverse cultural and geographic teams, aligning technical delivery with business and regulatory requirements.
Experience in integrated pharmaceutical IT environments, adept at translating complex business needs into compliant technical solutions.