Specialist IS Business Analyst
- Company: Amgen
- Location: India - Hyderabad
- Work mode: On-site
- Job type: Full-Time
- Posted: 2026-09-15
CAREER CATEGORY
Information Systems
JOB DESCRIPTION
Position Summary
Lead the validation team in a GMP High Salesforce application and serve as the accountable leader for validation governance, GxP compliance, RTM traceability, inspection readiness, and quality oversight. Drive compliant delivery through strong validation leadership, risk-based decision making, and operational excellence while developing a high-performing validation team.
Key Responsibilities
* Lead validation strategy, governance, and execution for GxP-regulated applications, computerized systems, and digital platforms.
* Ownership & oversight for validation activities, ensuring compliance with internal SOPs, regulatory requirements, and industry standards.
* Author & ownership of validation deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ Protocols, Validation Summary Reports (VSRs), and Requirements Traceability Matrices (RTMs).
* Establish and maintain end-to-end traceability between requirements, risks, test evidence, defects, and compliance documentation through RTM governance.
* Ensure inspection of readiness and support internal audits, regulatory inspections, CAPA, deviation management, and change control activities.
* Complete ownership of validation strategy, testing scope and end-to-end system validation.
* Lead and mentor Validation Engineers, establishing best practices and driving a quality-first culture.
* Partner with Product, Business, Quality, Regulatory, and Technology teams to support compliant and timely delivery of business initiatives.
* Drive continuous improvement initiatives to reduce validation cycle time while maintaining compliance and quality standards.
Basic Qualifications
* Bachelor's or Master's degree in Computer Science, Engineering, Information Systems, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related discipline.
* 8+ years of experience in Computer System Validation (CSV), Quality Assurance, or GxP-regulated environments.
* 3+ years of experience leading validation teams, validation programs, or quality compliance initiatives.
* Experience supporting regulated systems throughout the software development lifecycle (SDLC).
Preferred Qualifications
* Experience leading validation activities for global, enterprise-scale digital platforms.
* Experience implementing Computer Software Assurance (CSA) and risk-based validation methodologies.
* Experience validating cloud-based and SaaS platforms.
* Experience supporting Agile and product-centric delivery organizations.
* Experience driving validation automation and digital transformation initiatives in Life Sciences domain.
Required Skills
* Computer System Validation (CSV) expertise.
* Strong knowledge of GxP regulations, FDA 21 CFR Part 11, Annex 11, and Data Integrity requirements.
* Validation lifecycle management including Validation Plans, Risk Assessments, RTM, IQ/OQ/PQ, and VSRs.
* Requirements Traceability Matrix (RTM) creation, governance, and compliance management.
* Risk-based validation and test strategy development.
* Audit and inspection readiness management.
* Quality Management Systems (QMS), CAPA, deviation, and change control processes.
* Validation management tools such as ALM, Jira, Validation Management (VM), or equivalent platforms.
Good-to-Have Skills
* Computer Software Assurance (CSA).
* GAMP 5 methodology.
* Validation of Salesforce, Mulesoft, cloud, and SaaS solutions.
* Automated testing and validation frameworks.
* DevOps, CI/CD, and release management practices.
* Quality metrics, KPI reporting, and trend analysis.
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