Validation Engineer

Capgemini Engineering

Fundão

Híbrido

EUR 35 000 - 55 000

Tempo integral

14 dias+

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Vantagens oferecidas por esta oferta de emprego

Health and life insurance
Training and certifications in cutting-edge technologies
Referral program with bonuses
Career growth opportunities

Resumo da oferta

Capgemini Engineering in Fundão, Portugal is looking for a professional specialized in Computer System Validation (CSV) to ensure compliance with GxP guidelines. You will plan, define, and execute CSV activities and develop essential validation documentation.

The ideal candidate has a relevant academic background, strong experience in regulated environments, and excellent communication skills. The role offers a hybrid working model and emphasizes career growth in a supportive atmosphere.

Qualificações

  • Strong experience in Computer System Validation (CSV) within regulated environments.
  • Hands-on expertise in validation lifecycle activities (URS, FS/DS, IQ/OQ/PQ).
  • Proven ability to ensure full traceability and high-quality documentation.

Responsabilidades

  • Plan, define, and execute Computer System Validation (CSV) activities.
  • Develop and maintain validation documentation, including Validation Plans and User Requirement Specifications.
  • Translate business and regulatory requirements into validation deliverables.

Conhecimentos

Computer System Validation (CSV)
GxP compliance standards
Strong communication skills
Detail-oriented approach
Fluency in English

Formação académica

Degree in Pharmaceutical Sciences, Life Sciences, Engineering, or a related field

Descrição da oferta de emprego

Your Role

Plan, define, and execute Computer System Validation (CSV) activities in compliance with GxP guidelines (e.g., GAMP5, FDA, EMA). Develop and maintain validation documentation, including:

  • Validation Plans (VP)
  • User Requirement Specifications (URS)
  • Functional and Design Specifications (FS/DS)
  • IQ/OQ/PQ protocols and reports
Your Profile
  • 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, with solid knowledge of GxP, GAMP5, and compliance standards
  • Proven 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
  • Comfortable working in international, multicultural teams, with strong communication skills and fluency in English
What You'll Love About Working Here
  • Join a multicultural and inclusive team environment.
  • Enjoy a supportive atmosphere promoting work life balance.
  • Hybrid work.
  • Your career growth is central to our mission. Our array of career growth programs and diverse professionals are crafted to support you in exploring a world of opportunities.
  • Access valuable training and certifications in cutting edge technologies.
  • Engage in exciting national and international projects.
  • Health and life insurance.
  • Referral program with bonuses for talent recommendations.
  • Great office locations.
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