Computer System Validation Engineer
Validation engineer for regulated pharma (GxP) systems: owns validation strategy, risk assessment, IQ/OQ testing, change control, CAPA and audit readiness using GAMP 5/CSA, covering SaaS/cloud-hosted and AI/ML-enabled systems, with pharmacovigilance process knowledge and eLearning platform support. Onsite in Hyderabad or Bengaluru, 11 AM-8 PM.
- Compensation
- Not disclosed
- Location
- Hyderabad; Bengaluru
- Work setup
- Hybrid
- Seniority
- Not specified
- Employment
- Full time
- Experience
- 3+ years
- Category
- Industrial engineering
- Posted
Skills
Must have
- 3-8 years of experience
- Owns validation approach, risk assessment, scope, and testing strategy using GAMP 5 / CSA principles
- Manages validation deliverables, deviations, change control, CAPA support, traceability, and audit readiness
- Applies GxP expectations, GAMP 5, and CSA guidance across traditional, agile, and modern digital platforms
- Oversees validation of SaaS and cloud-hosted applications, including vendor assessment and shared responsibility
- Ensures controls around audit trails, access, ALCOA+, data lineage, and integrity risks
- Understands validation needs for AI/ML-enabled systems (intended use, data quality, explainability, drift monitoring, human oversight, revalidation triggers)
- Understanding of PV processes, system workflows, regulatory expectations, and documentation
- Cloud platform knowledge and underlying services/tech stack for qualification
- Experience with IQ/OQ execution, user story creation, validation, testing, and change management
- Ability to drive stakeholder follow-ups and keep deliverables on track
Nice to have
- Training development and content authoring
- Hands-on experience with eLearning platforms
Full description
Job Title: Computer System Validation-GxP
Description:
Timings : 11:00 AM - 8:00 PM
Owns validation approach, risk assessment, scope, and testing strategy using GAMP 5 / CSA principles to ensure effort is focused on patient safety, product quality, and data integrity. Manages validation deliverables, deviations, change control, CAPA support, traceability, and audit readiness to maintain the validated state of regulated systems. Applies GxP expectations, GAMP 5 , and CSA guidance across traditional, agile, and modern digital platforms, including knowing when supplier documentation can be leveraged Oversees validation of SaaS and cloud-hosted applications, including vendor assessment, shared-responsibility understanding, release impact review, and use of supplier evidence and quality agreements. Ensures controls around audit trails, access, ALCOA+, data lineage, and integrity risks across interfaces, manual processes, and connected systems. Understands validation needs for AI/ML-enabled systems, including intended use, data quality, explainability, drift monitoring, human oversight, and revalidation triggers. understanding of PV processes, system workflows, regulatory expectations, documentation and support for validation lifecycle activities Cloud platform knowledge, and underlying services/tech stack for qualification, manages qualification deliverables, change control, specifications, traceability to maintain the qualified state Process knowledge of GxP frameworks and coordination across applications/systems undergoing GxP validation activities; Experience with IQ/OQ execution, user story creation, validation, testing, and change management; Ability to drive stakeholder follow-ups and keep deliverables on track; Training development and content authoring; eLearning Platform Support: Hands-on experience with eLearning platforms; Understanding of typical patterns and challenges in building and sustaining these platforms from a project management perspective