CQV Engineer – QC Labs

QCS Staffing; Singapore; On-site; SGD 90,000 - 150,000; Full time

Job summary

QCS Staffing seeks a CQV Engineer to lead qualification efforts in QC labs for a life sciences project in Singapore. The role focuses on IQ/OQ/PQ execution, documentation, and collaboration with QA, QC, and vendor teams to ensure compliant equipment qualification.

You will qualify a range of analytical instruments (HPLC/UHPLC, GC, UV-Vis, pH meters) and support calibration, risk assessments, and change controls in a regulated manufacturing environment over a 24-month contract.

Qualifications

• Bachelor’s degree in engineering, life sciences, or related discipline.
• Extensive CQV experience in qualification and validation of analytical and QC lab equipment.
• Strong GMP knowledge and data integrity principles (ALCOA+).
• Ability to author qualification documentation and collaborate with QA/QC/Engineering and vendors.

Responsibilities

• Develop, execute, and document IQ, OQ, and PQ protocols for laboratory equipment in GMP environments.
• Commission and qualify laboratory equipment including HPLC/UHPLC, GC, UV-Vis, pH meters, balances, incubators, ovens and refrigerators.
• Prepare and review qualification protocols, risk assessments, reports, deviations, CAPAs and change controls under GMP and data integrity requirements.
• Support FAT/SAT/calibration and vendor management in collaboration with QA, QC, Engineering and suppliers.

Skills

CQV Engineering

IQ/OQ/PQ

GMP

Data Integrity (ALCOA+)

HPLC/UHPLC

Education

Bachelor’s degree in engineering or life sciences

Tools

Laboratory equipment qualification

Job description

CQV Engineer – QC Labs – Singapore – 24-Month Contract – Life Sciences

How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!

Our client is currently seeking the skills of a CQV Engineer to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!

What You’ll Deliver

• Develop, execute, and document IQ, OQ, and PQ protocols for analytical and QC laboratory equipment in GMP-regulated environments.
• Commission and qualify a range of laboratory equipment including HPLC/UHPLC, GC, UV-Vis Spectrophotometers, TOC Analyzers, Dissolution Systems, pH/Conductivity Meters, Balances, Incubators, Ovens, and Refrigerators.
• Prepare and review qualification protocols, risk assessments, summary reports, deviations, CAPAs, change controls, and temperature mapping studies while ensuring compliance with GMP and Data Integrity requirements.
• Support FAT, SAT, calibration, and vendor management activities while working closely with QA, QC, Engineering, and external suppliers to ensure successful and timely project completion.

Experience required:

• Bachelor’s degree in engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, or a related discipline.
• Extensive CQV experience involving qualification and validation of analytical and QC laboratory equipment within pharmaceutical, biotech, or regulated manufacturing environments.
• Strong understanding of GMP requirements, Data Integrity principles (ALCOA+), and equipment qualification lifecycle processes.
• Demonstrated ability to author technical qualification documentation, manage compliance activities, solve technical issues, and effectively collaborate with QA, QC, Engineering teams, and equipment vendors.