Our client, a renowned international engineering and commissioning firm, is at the forefront of designing and delivering cutting-edge life sciences and manufacturing facilities across Asia. As demand for healthcare products surges in Japan, they are growing rapidly and now seek a CQV Engineer to support major pharmaceutical projects in Osaka.

In this role, you’ll lead commissioning, qualification, and validation activities for GMP-critical systems—from clean utilities and HVAC to packaging and production equipment. You’ll be hands-on with everything from protocol execution (IQ/OQ/PQ) to documentation and regulatory compliance, ensuring systems are delivered safely, efficiently, and to the highest global standards.

You’ll collaborate with multidisciplinary teams and serve as a key interface between international stakeholders and local project execution. A background in engineering (Chemical, Mechanical, Bioprocess, or similar), strong communication skills, and experience in GMP-regulated environments are essential. Japanese and English language capabilities are highly valued.

This is a unique opportunity to make an impact on the future of healthcare manufacturing in Japan, while working with one of the industry’s most respected consultancies.

To explore further, reach out to Stevan Kottritsch at Invenio Global.
EA Personnel KAH Registration No: R1108948
EA Licence No: 19S9800