CIP Engineer: CQV & GMP Systems Expert

Hyde Engineering + Consulting; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Hyde Engineering + Consulting in Singapore is seeking a CIP Engineer (Clean-in-Place) to lead design reviews, commissioning, qualification, validation, and lifecycle management of CIP systems in pharmaceutical and biopharmaceutical facilities.

You will support project execution from Concept Design through OQ/PQ/CPV, review P&ID, process flows, and automation, and coordinate CQV documentation with QA, Manufacturing, and Validation teams.

Qualifications

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

Responsibilities

• Review CIP system designs for pharmaceutical and biopharmaceutical manufacturing 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.
• Coordinate CQV activities: IQ, OQ, PQ, validation protocols and VSRs.
• Support traceability matrix development and management.
• Coordinate punch-list resolution and CQV documentation closure.
• Support cleaning validation strategy development and sampling activities.

Skills

CIP design and operation

Cleaning validation principles

Commissioning and Qualification

GMP regulations

P&ID review

FAT/SAT execution

Technical report writing

Education

Bachelor's Degree in Chemical/Mechanical/Bioprocess/Process Engineering

Pharmaceutical Engineering or related discipline

Job description

Hyde Engineering + Consulting in Singapore is seeking a CIP Engineer (Clean-in-Place) to lead design reviews, commissioning, qualification, validation, and lifecycle management of CIP systems in pharmaceutical and biopharmaceutical facilities.

You will support project execution from Concept Design through OQ/PQ/CPV, review P&ID, process flows, and automation, and coordinate CQV documentation with QA, Manufacturing, and Validation teams.