Inactive
C

Capgemini

Global consulting, technology services, outsourcing

CQV / Validation / Process Engineering - Aerospace

Validation, Compliance & Quality SystemsPosted on Aug 3
Full-timeNo salary listed

About the Job

Requirements

  • Academic background in Engineering, Biotechnology, Bioengineering, Biomedical Engineering, Biomedical Sciences, Pharmacy, or another relevant technical/scientific field.
  • At least 3 years of professional experience in one or more of Commissioning & Qualification (CQV/C&Q), Validation / Process Validation, Process Engineering, Manufacturing Engineering, Industrialization, or Quality Engineering.
  • Professional experience within Aerospace/Aeronautics and/or Life Sciences, including Pharmaceutical, Biotechnology, or Medical Devices environments.
  • Experience with validation, qualification, testing, commissioning, or industrial process activities, according to the relevant industry.
  • Experience preparing and maintaining technical documentation, protocols, reports, procedures, test evidence, and/or engineering documentation.
  • Good level of English.

Responsibilities

  • Support commissioning, qualification, validation, and/or process engineering activities within regulated and quality-driven environments.
  • Prepare, review, execute, and maintain technical, validation, and qualification documentation, ensuring compliance with applicable procedures, SOPs, quality standards, and project requirements.
  • Prepare and execute qualification and validation protocols, test cases, reports, and supporting evidence, including IQ/OQ/PQ activities where applicable.
  • Support industrialization, process validation, process optimization, and manufacturing engineering activities.
  • Participate in FAT and SAT activities, including remote support when required.
  • Support deviation and test incident management, investigation, root cause analysis, and definition of follow-up actions.
  • Contribute to CAPA, change control, and risk assessment activities, according to project and industry requirements.
  • Support the development, standardization, and continuous improvement of manufacturing and engineering processes.
  • Work with electronic validation, qualification, documentation, or quality management systems, such as Kneat or equivalent tools, depending on the project.
  • Collaborate with multidisciplinary and international teams, ensuring effective communication between Engineering, Manufacturing, Quality, and other project stakeholders.
  • Participate in regular project follow-up meetings, report progress, and ensure that documentation and project trackers remain up to date.

Desired Qualifications

  • Knowledge of methodologies such as IQ/OQ/PQ, risk assessment, root cause analysis, CAPA, change control, deviations, PFMEA, or continuous improvement is valued.
  • Experience with electronic validation, documentation, or quality management systems is an advantage.

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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