Not specified (potentially hybrid or onsite depending on project requirements).
Computer system validation experience
Equipment qualification fat sat iq oq pq
Clean utilities validation execution
PM ASIA PROJECT SERVICES PTE. LTD. is seeking a CQV Engineer to support pharmaceutical clients in commissioning, qualification, and validation activities related to manufacturing process equipment. The ideal candidate should possess significant experience in equipment qualification and validation documentation, with a strong focus on attention to detail and compliance with industry standards
Job Summary
This role supports a pharmaceutical client by planning and coordinating commissioning, qualification, and validation activities for various manufacturing processes.
The engineer is responsible for creating, reviewing, and approving validation lifecycle documents including protocols and reports for equipment and analytical instruments.
Candidates must be able to lead investigations regarding discrepancies identified during qualification activities within a strict cGMP environment.
Matching Summary
Match Score: 85
PM ASIA PROJECT SERVICES PTE. LTD. is seeking a CQV Engineer to support pharmaceutical clients in commissioning, qualification, and validation activities related to manufacturing process equipment. The ideal candidate should possess significant experience in equipment qualification and validation documentation, with a strong focus on attention to detail and compliance with industry standards.
Skills & Requirements
Must-have
Computer System Validation experience
Equipment Qualification FAT SAT IQ OQ PQ
Clean Utilities Validation execution
Cleaning validation in cGMP environment
Risk assessment documentation creation
Nice-to-have
ASTM2500 process equipment knowledge
Ultrafiltration units experience
Chromatography column expertise
Leading cross-functional investigation meetings
COTS analytical instruments lifecycle management
Key Requirements
Experience in Pharmaceutical or BioPharma industries