CQV Documentation Lead — BioPharma Validation Expert

Process Engineering Specialists in Singapore is seeking a CQV Doc Prep Lead to develop and review CQV lifecycle documents for various projects in the Life Sciences industry. Responsibilities include authoring validation protocols, ensuring compliance with GMP regulations, and maintaining audit-ready documentation.

The position requires collaboration with engineers, QA, and cross-functional teams, and may involve occasional travel to Malaysia. A strong background in documentation and validation is essential for success in this role.