Data Validation Expert
2 semanas atrás
About Us
Capgemini Engineering, part of the Capgemini Group, empowers individuals and organizations to achieve more. Our culture is centered on growth mindset, diversity, inclusion, inspiring excellence, and teamwork. We create life-changing innovations impacting billions worldwide.
We have over 270,000 team members across nearly 50 countries in sectors like aeronautics, automotive, communications, energy, life sciences, software & internet, space & defense, and consumer products.
About the Position
We seek a partner who shares knowledge, responsibility, and commitment in executing activities related to day-to-day business operations, specifically in CSV/QA areas.
This position is open for Lisbon, Porto, and Fundão. Your role will be to:
- Support computerized system validation and IT qualification of applications and software.
- Anticipate and advise on GxP-regulated and regulatory compliance computerized validation processes based on each system's specifications.
- Perform QA activities supporting Medical Devices software development projects.
- Perform end-to-end validation to verify software (validation planning, test protocols and reports, risk assessments).
- Work within a team following regulations and guidelines, interacting with other teams and stakeholders.
- Share knowledge about computerized system validation and medical devices.
Your Profile
We're looking for someone with an academic degree in biomedical engineering, pharmaceutical sciences, IT, or computer science, or related fields. Previous experience in computerized system validation – CSV, ideally 2 to 5 years, is required. Strong knowledge of GxP regulations and guidelines is necessary. Solid verbal and written communication skills in English (at least B2) are also essential.
Salary Information
The estimated salary for this position is around €60,000 - €80,000 per year, depending on location and experience. This figure is based on industry standards and market conditions in Portugal.
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