CIP Engineer - CQV for Pharma Facilities (12-mo Contract)

Leap29; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

Leap29 is seeking a CIP Engineer to oversee design review, commissioning, qualification, validation, and lifecycle management of CIP systems in pharmaceutical and biotech facilities. The role combines engineering and CQV expertise to ensure compliant, tested, and validated CIP processes across sterile manufacturing environments.

The successful candidate will support Concept through OQ, PQ, and CPV, collaborating with QA, QC, and Validation teams to achieve on-time delivery and regulatory

Qualifications

• 5–10 years in pharmaceutical or biopharmaceutical engineering and CQV.
• Minimum 3 years direct CIP engineering and qualification experience.
• Experience with GMP regulated facilities including biologics, vaccines, sterile manufacturing, OSD API.
• Proven experience executing CQV protocols and validation documentation.

Responsibilities

• Review CIP system design for pharmaceutical and biopharmaceutical facilities.
• Evaluate P&IDs, process flow diagrams, equipment layouts, and automation sequences related to CIP systems.
• Verify CIP system design against process requirements, product contact surfaces, cleanability, and regulatory expectations.
• Support FAT, SAT, and vendor package reviews.
• Conduct hydraulic and process evaluations to ensure adequate flow, velocity, turbulence, and coverage.
• Identify opportunities for CIP cycle optimization to reduce water, chemical consumption, and cycle times.
• Support troubleshooting of CIP failures and cleaning effectiveness issues.

Skills

CQV experience

CIP design

P&ID review

GMP knowledge

Validation documentation

Education

Bachelor's in Chemical Engineering

Bachelor's in Mechanical Engineering

Bioprocess Engineering

Job description

Leap29 is seeking a CIP Engineer to oversee design review, commissioning, qualification, validation, and lifecycle management of CIP systems in pharmaceutical and biotech facilities. The role combines engineering and CQV expertise to ensure compliant, tested, and validated CIP processes across sterile manufacturing environments.

The successful candidate will support Concept through OQ, PQ, and CPV, collaborating with QA, QC, and Validation teams to achieve on-time delivery and regulatory