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Tier-1 pharma brand, metro Bangalore location, but role is niche LIMS with senior requirement.
Highly specialized in pharma LIMS, CSV and GxP, making skills less transferable across industries.
Explicit 12+ years, mandatory LabVantage LIMS experience and CSV/GxP regulatory requirements restrict candidates.
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Lead end-to-end delivery of global LabVantage LIMS implementation, upgrades, integrations, releases, and validation in a GxP-regulated pharmaceutical environment.
Own project plans, budgets, and compliance with Quality Management System and act as Quality representative throughout project phases, including reviewing validation and risk documentation.
Drive adoption of IT DevOps automation and AI technologies to accelerate releases, support incident management, data integrity, and coordinate regulatory audit responses.
Bachelor's degree in Computer Science, Information Technology or related field.
Minimum 12 years professional experience in software development with at least 6 years as Technical Project Manager specifically for LabVantage LIMS (version 8.5 or higher) in a regulated Life Sciences setting.
Significant pharmaceutical industry experience, specifically with Computer Systems Validation (CSV) and regulatory knowledge including GxP, GAMP 5, and 21 CFR Part 11.
Proven expertise in LIMS development and system integrations using RESTful APIs, SOAP services, and middleware platforms (e.g. MuleSoft).
Experienced technical leader with deep LabVantage LIMS and CSV expertise able to influence multi-geography stakeholders in a global life sciences context.
Strong skills in stakeholder management spanning laboratory users, Quality, IT, vendors, and integration partners, able to translate business needs into technical solutions.
Comfortable working in a culturally diverse environment with excellent English communication and coordination skills across time zones.