Job Title: CQV Validation Engineer 

Experience: 2+ years

Qualification: This is a professional position, and as such, we require, at minimum, a Bachelor’s degree in Engineering include Mechanical, Electrical, Industrial, Petroleum, Process, Structural, Chemical, Mining, Computer Science Engineering or advanced educational background equating to the U.S. equivalent of a Bachelor’s degree in one of the aforementioned subjects.

Job Description: 

Execute commissioning and qualification protocols (IQ/OQ/PQ) for GMP manufacturing equipment, utilities, and facility systems.
Support protocol development, review, and execution in accordance with regulatory  and company quality standards.
Perform field verification, testing, and troubleshooting during commissioning and  qualification activities.
Coordinate with engineering, quality, manufacturing, and project teams to ensure successful system turnover.
Review vendor documentation, FAT/SAT packages, and engineering design documentation.
Support deviation investigations, change control, and CAPA activities related to CQV work.
Ensure compliance with cGMP, FDA, and global regulatory requirements.
Assist with documentation packages and system turnover to operations.