QC Specialist - Method Development & GMP Excellence

GMP Technologies; Singapore; On-site; SGD 67,000 - 100,000; Full time

Job summary

GMP Technologies in Tuas, Singapore is seeking a QC Specialist for a minimum 6 months to support QC testing activities, method development, validation, and equipment qualification. The role requires strong knowledge of cGMP and regulatory expectations.

You will work with SAP, LES, and laboratory systems, handling deviation investigations, CAPA, and change controls, while contributing to continuous improvement and data integrity across QC processes.

Qualifications

• Degree in Chemistry, Biology, Life Sciences, or related scientific discipline with relevant QC laboratory experience.

Responsibilities

• Provide technical support to QC testing teams on analytical activities including method development, qualification, validation, verification, transfer, and equipment qualification.
• Support analytical method performance monitoring, troubleshooting, and provide QC SME guidance.
• Manage QC reagent qualification and stability programs, monitor results and trends, support corrective actions.
• Provide technical support for QC computerized systems such as SAP, LES, and laboratory systems including updates and master data changes.
• Support GMP quality activities including deviation investigations, CAPA, change controls, SOP/document review, and audit readiness.
• Support data integrity, documentation compliance, and regulatory requirements in line with cGMP and company procedures.
• Lead or support QC projects and continuous improvement initiatives within the team.

Skills

QC testing

Analytical methods

SOP/document reviews

Communication

Education

Bachelor's degree in Chemistry/ Biology/ Life Sciences

Tools

SAP

LES

Laboratory systems

Job description

GMP Technologies in Tuas, Singapore is seeking a QC Specialist for a minimum 6 months to support QC testing activities, method development, validation, and equipment qualification. The role requires strong knowledge of cGMP and regulatory expectations.

You will work with SAP, LES, and laboratory systems, handling deviation investigations, CAPA, and change controls, while contributing to continuous improvement and data integrity across QC processes.