CSV Engineer — Global Pharma Validation
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Your Role
As a Computer System Validation (CSV) Engineer, you will play a key role in ensuring that computerized systems used in regulated environments meet compliance standards and operate as intended.
You will collaborate with cross-functional teams to develop and execute validation strategies that align with industry regulations.
In this role you will play a key role in:
- Developing and executing validation protocols in pharmaceutical environments
- Implementing ISPE GAMP5 principles within quality, operational, and project contexts
- Analyzing and validating a wide range of technical systems, including automated systems in regulated environments
- Minimum 3 years experience in validation and qualification in the pharmaceutical industry (FDA, Eudralex, WHO) or equivalent environments (food, cosmetics)
- Strong knowledge of ISPE GAMP5 principles applied to quality, operational and project contexts
- Excellent analytical skills to actively contribute to validation strategies and CSV activities
- Fluency in both French and English (written and spoken)
- Career acceleration programs – From associate to leaders and beyond, get support in your career at every stage with award-winning programs such as our leadership development program, Connected Manager, to accelerate your growth and develop your expertise.
- Continuous feedback – We take a human-centric approach to foster growth and performance. Our performance management tool GetSuccess enables continuous feedback, quarterly check-ins with managers, and ongoing performance discussions.
- FlexAbroad – Employees in 20+ countries can work abroad for up to 45 days in a 12-month period.
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