C&Q Engineer for Single-Use Systems

AMARIS GROUP SA; Singapore; On-site; SGD 70,000 - 90,000; Full time

Benefits offered by this job

International community

Comprehensive training program

Team events

Job summary

Amaris Consulting in Singapore is seeking a life sciences professional to support commissioning and qualification activities for single-use systems and materials. You will prepare, execute, and review C&Q protocols, verify specifications, and document discrepancies while coordinating with Engineering, Manufacturing, Validation, and Quality teams to ensure GMP-compliant readiness.

The role emphasizes independent work and strong documentation, with collaboration across technical and quality groups

Qualifications

• Bachelor’s degree in relevant life sciences field or equivalent
• 3+ years in commissioning and qualification in pharma/biotech environments
• Hands-on with single-use systems and materials
• Experience preparing and executing qualification protocols and maintaining documentation
• Good understanding of GMP requirements and qualification processes

Responsibilities

• Support commissioning and qualification activities for single-use systems and materials
• Prepare, execute, and review C&Q protocols and supporting documentation
• Verify that single-use systems and materials meet defined specifications and qualification requirements
• Document and support investigation and resolution of discrepancies during C&Q activities
• Coordinate with Engineering, Manufacturing, Validation, and Quality teams to deliver C&Q activities
• Support change-control activities related to single-use systems and materials
• Ensure activities follow site procedures and GMP requirements

Skills

GMP knowledge

Technical documentation

Independent working

Cross-functional collaboration

English fluency

Education

Bachelor’s degree in Chemical Engineering, Biotechnology, Pharmaceutical Sciences, Life Sciences

Tools

Qualification protocols

Job description

Amaris Consulting in Singapore is seeking a life sciences professional to support commissioning and qualification activities for single-use systems and materials. You will prepare, execute, and review C&Q protocols, verify specifications, and document discrepancies while coordinating with Engineering, Manufacturing, Validation, and Quality teams to ensure GMP-compliant readiness.

The role emphasizes independent work and strong documentation, with collaboration across technical and quality groups