Vacancy description
Principal Programming Analyst in Bombay, भारत
Thermo Fisher Scientific
Bombay, भारत
Principal Programmer Analyst role supporting Pharmacovigilance system implementations and Computer System Validation at a life-sciences technology company. Leads complex validation strategies, ensures regulatory compliance, and drives process improvements across clinical trial and drug safety systems.
Responsibilities
- Lead validation strategies and oversight for PV system implementations, upgrades, and complex technical enhancements
- Define requirements with stakeholders and ensure translation into testable, compliant functional specifications
- Plan, author, and execute system testing activities including SIT, UAT, and performance qualification
- Own validation deliverables including plans, specifications, test protocols, and compliance documentation
- Drive continuous improvement and standardization initiatives across PV validation processes
Requirements
- Expert-level knowledge of Computer System Validation (CSV) and GxP regulations
- Deep experience with Pharmacovigilance systems and 21 CFR Part 11 compliance
- Proven ability to lead requirements definition and risk-based validation strategies
- Strong technical acumen in system integrations, data migrations, and testing methodologies
- Experience mentoring validation professionals and cross-functional technical teams
- Knowledge of AI and automation applications in validated environments
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