Inactive
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Capgemini

Global consulting, technology services, outsourcing

CSV & Computerized Systems Validation Pharmaceutical

Regulatory & Quality (Life Sciences)Posted on Aug 3
Full-timeLyon, FranceNo salary listedIn-person

About the Job

Requirements

  • A degree from an engineering school or Bac+5 training in computer science, quality, processes, or an equivalent field is required.
  • Two to five years of experience in computerized systems validation (CSV) in the pharmaceutical industry or a regulated environment is required.
  • Knowledge of GAMP 5, GMP, and data integrity is required.
  • Professional written and spoken English is required.

Responsibilities

  • Perform risk analyses of computerized systems and data flows.
  • Ensure validation activities comply with quality and regulatory standards.
  • Write validation plans, IQ/OQ protocols, and associated reports.
  • Track changes, deviations, and non-conformities.
  • Help maintain regulatory compliance for systems subject to GAMP 5 and 21 CFR Part 11 requirements.

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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