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Capgemini

Global consulting, technology services, outsourcing

CSV Engineer - Lifesciences & Medical Devices

Regulatory & Quality (Life Sciences)Updated on Nov 14
Full-time

About the Job

Requirements

  • Academic background in Pharmaceutical Sciences, Life Sciences, Engineering, or a related field, ensuring understanding of regulated environments and industry practices.
  • Strong experience in Computer System Validation (CSV) within regulated environments such as pharmaceutical or biotech, with solid knowledge of GxP, GAMP5, and compliance standards.
  • Ability to translate business and regulatory requirements into validation deliverables, ensuring full traceability and high-quality documentation.
  • Hands-on expertise in validation lifecycle activities (URS, FS/DS, IQ/OQ/PQ) combined with a structured and detail-oriented approach.
  • Fluency in English.

Responsibilities

  • Plan, define, and execute Computer System Validation (CSV) activities in compliance with GxP guidelines, including GAMP5, FDA, and EMA requirements.
  • Develop and maintain validation documentation, including Validation Plans (VP), User Requirement Specifications (URS), Functional and Design Specifications (FS/DS), and IQ/OQ/PQ protocols and reports.

About the Company

Capgemini

Global consulting, technology services, outsourcing

Capgemini provides consulting, technology services, and outsourcing to help organizations transform digitally. Its offerings include strategy and transformation consulting, system integration, application development, IT infrastructure management, and managed IT operations. It differentiates itself with a global presence in over 50 countries and a focus on applying AI, cloud, and cybersecurity to real business problems. Its goal is to help clients navigate digital transformation and improve efficiency and innovation through tailored, contract-based or managed services.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1967

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