Not specified (assumed onsite based on the nature of the role)
Cqv in pharmaceutical industry
Gmp guidelines compliance
Ispe baseline guides knowledge
LANYOU TECH PTE. LTD. is seeking a Senior CQV Engineer based in Singapore, responsible for the commissioning, qualification, and validation of cleanroom and process systems in compliance with regulatory standards. The ideal candidate should possess at least 8 years of experience in the pharmaceutical or biotech industry and strong knowledge of GMP guidelines
Job Summary
The CQV Engineer is responsible for the commissioning, qualification, and validation of CU/Cleanroom/Temperature Controlled Unit/Process systems.
This role ensures that all systems are installed, tested, and qualified in strict compliance with cGMP and regulatory requirements.
Candidates must possess strong documentation skills and the ability to work independently within a cross-functional project team.
Matching Summary
Match Score: 85
LANYOU TECH PTE. LTD. is seeking a Senior CQV Engineer based in Singapore, responsible for the commissioning, qualification, and validation of cleanroom and process systems in compliance with regulatory standards. The ideal candidate should possess at least 8 years of experience in the pharmaceutical or biotech industry and strong knowledge of GMP guidelines.
Skills & Requirements
Must-have
CQV in pharmaceutical industry
GMP guidelines compliance
ISPE Baseline Guides knowledge
USP/EP and ASTM E2500 standards
Annex 15 regulatory requirements
Nice-to-have
Strong problem-solving skills
Cross-functional team collaboration
Independent work capability
Stakeholder communication skills
Chinese language proficiency
Key Requirements
Bachelors Degree in Engineering or Life Sciences
8 years experience of CQV in pharmaceutical/biotech
Strong knowledge of GMP guidelines and ISPE Baseline Guides