Pharma QC Specialist: Validation, ALCOA+, Troubleshooting

GMP Technologies; Singapore; On-site; SGD 36,000 - 60,000; Full time

Job summary

GMP Technologies (S) Pte Ltd in Singapore is seeking a QC Associate to perform routine chemical testing of raw materials and utilities, and to support manufacturing processes.

The role requires hands-on QC laboratory experience in pharma, familiarity with ALCOA+, GMP/GLP, and readiness to provide weekend support. You will contribute to validation and transfer activities, CAPA investigations, and documentation maintenance.

Qualifications

• Diploma/Degree in Chemistry, Pharmaceutical Science, Life Sciences or related discipline.
• Hands-on experience in pharmaceutical/biopharmaceutical QC laboratory testing.
• Experience in raw material and/or utilities/water testing.
• Experience with TOC and conductivity testing preferred.
• Familiar with GMP/GLP and ALCOA+ principles.
• Experience in verification/validation/transfer, investigations or CAPA advantageous.
• Familiar with laboratory calibration and troubleshooting.
• Comfortable providing weekend support when required.

Responsibilities

• Perform routine chemical testing of raw materials and utilities/water samples.
• Perform testing to support manufacturing processes, process validation, cleaning validation, and reagent qualification.
• Support method verification, validation and transfer for projects and NPI.
• Ensure testing and documentation comply with ALCOA+, cGMP, cGDP and cGLP.
• Perform peer review of laboratory testing and data.
• Perform equipment troubleshooting, calibration, maintenance and verification.
• Support investigation of OOS, atypical/invalid results and equipment issues, including CAPA closure.
• Assist with preparation and periodic review of laboratory documentation and SOPs.
• Maintain laboratory inspection readiness, inventory and good housekeeping.
• Support continuous improvement and laboratory improvement activities.
• Provide ad-hoc weekend or off-office-hour support when required.

Skills

QC testing

ALCOA+

cGMP/GLP

TOC testing

Conductivity testing

Laboratory investigations

Education

Diploma/Degree in Chemistry, Pharmaceutical Science or Life Sciences

Tools

Calibration equipment

Job description

GMP Technologies (S) Pte Ltd in Singapore is seeking a QC Associate to perform routine chemical testing of raw materials and utilities, and to support manufacturing processes.

The role requires hands-on QC laboratory experience in pharma, familiarity with ALCOA+, GMP/GLP, and readiness to provide weekend support. You will contribute to validation and transfer activities, CAPA investigations, and documentation maintenance.