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open role · workday:amgen

Specialist IS Business Analyst

$AMGNHyderabad· posted 1d ago

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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requirements

• 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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