This role involves supporting pharmaceutical biologics clients in Singapore through full lifecycle facility modification and new equipment introduction
Job Summary
This role involves supporting pharmaceutical biologics clients in Singapore through full lifecycle facility modification and new equipment introduction.
The engineer will supervise contractor works, manage commissioning activities including IQ/OQ/PQ, and ensure compliance with cGMP standards.
Key responsibilities include coordinating FAT/SAT activities, maintaining project documentation, and acting as the primary interface between engineering, QA, and operations teams.
Matching Summary
Match Score: 85
This role involves supporting pharmaceutical biologics clients in Singapore through full lifecycle facility modification and new equipment introduction.
Skills & Requirements
Must-have
Facility modification projects in GMP environment
Equipment introduction and commissioning IQ/OQ/PQ
Contractor and vendor site supervision
Change control and validation documentation
Reading P&IDs and engineering drawings
Nice-to-have
Cross-functional stakeholder management skills
Experience with architectural M&E works
Strong risk assessment capabilities
Key Requirements
Degree or Diploma in Mechanical, Chemical, or Biomedical Engineering
Minimum 4 years of project engineering experience in pharmaceutical/biologics
Proven hands-on experience in GMP facility modifications and equipment qualification