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Capgemini

Global consulting, technology services, outsourcing

Ingénieure / Ingénieur AQ - Investigations d'Anomalies & Déviations CAPA, Industrie Pharmaceutique

Regulatory & Quality (Life Sciences)Updated on Nov 14
Full-timeNo salary listed

About the Job

Requirements

  • A Bac+5 degree in Engineering, Pharmacy, Biology, Chemistry, or equivalent is required.
  • At least five years of experience in production support, process support, or operational quality assurance in the pharmaceutical industry is required.
  • Confirmed experience in quality investigations, deviation management, and CAPA is mandatory.
  • Proficiency in Veeva Vault QMS (Event & CAPA) is mandatory.
  • Knowledge of GMP standards is required.
  • Knowledge of Data Integrity, Compliance, and Sterility Assurance is expected.
  • Professional English proficiency is required.

Responsibilities

  • Lead quality investigations related to deviations, anomalies, and quality events.
  • Identify root causes in collaboration with production teams.
  • Define and track corrective and preventive actions (CAPA).
  • Support teams on GMP compliance, Data Integrity, and sterility matters.
  • Contribute to audit preparation and continuous improvement of quality processes.

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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