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 in CQV, validation, or engineering within the pharmaceutical or biotechnology industry.
• Strong knowledge of GMP, validation principles, and regulatory requirements.
• Experience with process equipment, utilities (HVAC, WFI, clean steam, compressed air), and automation systems.
• Familiarity with ISPE Baseline Guides, GAMP 5, and ASTM E2500 methodologies.
• Fluent in English.

Soft skills

• Strong analytical and problem-solving skills, with attention to detail.
• Excellent communication skills and ability to work in cross-functional teams.

Why Join Us?

• Personalized support and resources to accelerate your career growth
• An open, diverse, and innovative ecosystem that empowers you to step out of your comfort zone
• The opportunity to become a company shareholder
• Engagement with community and non-profit technology projects
• Supportive policies for work-life balance and parenthood

Fortil is committed to equal opportunity. All our positions are open to people with disabilities, regardless of gender, origin, or sexual orientation.