Hello Network,
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.
If you are interested please send your CV to:
kainen.oragbade@g2recruitment.com