CQV Engineer
Share
Job Location:
Monthly Salary:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Fortil is an international engineering and technology consulting group built on an independent model bringing together over 2500 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.
Key Skills
- ASP.NET
- Health Education
- Fashion Designing
- Fiber
- Investigation
