CQV Engineer · On-site
Location:
Region: Antwerp
Country: Belgium
Role:
- Industry: Engineering
- Job Type: Contract / Freelance
Working Arrangement: On-site
Rate: Negotiable
Application Details:
- Date Posted:
Start Date: ASAP
Expiry Date: 30/04/2026
Job Reference: 10032613
CQV Engineer · On-site
We are seeking a detail-oriented CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning and qualification activities for process equipment within pharmaceuticals. The ideal candidate will ensure that equipment and systems are installed, tested, and documented in compliance with regulatory requirements and company standards.
Requirements:
- Lead and execute commissioning and qualification activities for process equipment.
- Develop and review validation documentation, including protocols, test scripts, and summary reports.
- Coordinate with engineering, quality assurance, and manufacturing teams to ensure timely project execution.
- Ensure compliance with GMP and regulatory standards (e.g., FDA, EMA).
- Support risk assessments (FMEA) and deviation investigations.
- Review vendor documentation, FAT/SAT documentation, and turnover packages.
- Provide on-site troubleshooting and technical support during startup and validation phases.
Your profile:
- Bachelor’s degree in Engineering (Chemical, Mechanical, Biomedical, or related field).
- 3+ years of CQV experience in pharmaceutical or biotech manufacturing.
- Strong knowledge of GMP, validation lifecycle, and regulatory requirements.
- Experience with process equipment qualification and documentation.
- Excellent communication and organizational skills.
g2 Recruitment are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law.