Pharma CIP Engineer | CQV & Validation Specialist

Hyde Engineering + Consulting, Inc.; Singapore; Hybrid; SGD 120,000 - 180,000; Full time

Job summary

Hyde Engineering + Consulting, Inc. is seeking a CIP Engineer to design, commission, qualify, validate, and optimize CIP systems in Singapore pharma facilities.

The role blends engineering and CQV to ensure systems meet cGMP, FDA, EU GMP Annex 1, ISPE, and internal standards while supporting CQV from Concept Design through CPV. Requirements include 5–10 years in pharma/CQV, 3+ years CIP experience, and strong skills in P&ID review, validation planning, and technical reporting.

Qualifications

• Bachelor’s degree in engineering related to pharma manufacturing.
• 5–10 years of pharma or biopharmaceutical engineering and CQV experience.
• Minimum 3 years direct CIP engineering and qualification experience.
• Experience with GMP regulated facilities including biologics, vaccines, sterile manufacturing, and OSDis.
• Proven CQV protocol execution and validation documentation experience.

Responsibilities

• Review CIP system designs for pharma/biopharma facilities and support design reviews.
• Evaluate P&IDs, process flows, equipment layouts, and automation sequences for CIP.
• Support FAT, SAT and vendor package reviews and resolve design gaps.
• Develop and execute CQV activities: CTPs, IQ, OQ, PQ, validation reports.
• Coordinate cleaning validation strategy, sampling, and data analysis.
• Review CIP automation logic and sequence of operations.

Education

Chemical Engineering

Mechanical Engineering

Bioprocess Engineering

Process Engineering

Pharmaceutical Engineering

Related Engineering Discipline

Tools

P&ID review

FAT/SAT execution

Technical report writing

GMP regulations

Job description

Hyde Engineering + Consulting, Inc. is seeking a CIP Engineer to design, commission, qualify, validate, and optimize CIP systems in Singapore pharma facilities.

The role blends engineering and CQV to ensure systems meet cGMP, FDA, EU GMP Annex 1, ISPE, and internal standards while supporting CQV from Concept Design through CPV. Requirements include 5–10 years in pharma/CQV, 3+ years CIP experience, and strong skills in P&ID review, validation planning, and technical reporting.