QC Specialist (Min. 6 months contract) | Pharma | Tuas

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

About the job QC Specialist (Min. 6 months contract) | Pharma | Tuas

Job Scope:

• 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 technical expertise as a subject matter expert (SME).
• Manage QC reagent qualification and stability programs, including monitoring results, trends, and supporting corrective actions.
• Provide technical support for QC computerized systems such as SAP, LES, and laboratory systems, including system updates, troubleshooting, master data changes, and implementation activities.
• 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 accordance with cGMP, quality standards, and company procedures.
• Lead/support QC projects, continuous improvement initiatives, knowledge transfer, and training activities within the team.

Requirements:

• Degree in Ch emistry, Biology, Life Sciences, or related scientific discipline with relevant QC laboratory experience (pharmaceutical/biologics industry preferred).
• Minimum 2 years of relevant experience for QC Specialist level; candidates with higher experience may be considered for Senior QC Specialist roles.
• Experience in analytical testing activities including method validation, qualification, verification, method transfer, stability studies, and equipment qualification.
• Good understanding of cGMP requirements , QC laboratory practices, and regulatory expectations.
• Familiarity with QC systems and computerized systems such as SAP, LES, laboratory systems , and related master data management activities.
• Experience supporting investigations, deviations, CAPA, change controls, SOP/document review, and audit readiness activities.
• Strong analytical, problem-solving, and communication skills with the ability to work independently and collaborate with cross-functional te ams

We regret that only shortlisted candidates will be notified.