Job Description
Fortil is an international engineering and technology consulting group, built on an independent model, bringing together over 2,500 employees. With 30 offices across 14 countries, Fortil fosters entrepreneurial freedom and the empowerment of individual potential.
Your Responsabilities
As a CQV Engineer you will play a key role in ensuring that all equipment, systems, and facilities used in manufacturing are properly commissioned, qualified, and validated according to GMP regulations.
You will be responsible for managing CQV activities for new projects, modifications, and ongoing operations, ensuring compliance and operational readiness of all systems.
Your Profile
- Degree in Chemical, Mechanical, or Biomedical Engineering, Pharmacy, or related field.
- +2 years of experience
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