QC Validation & Transfer Lead - Biopharma Projects

GlaxoSmithKline plc; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

GSK Tuas Vaccines is seeking a QC Specialist to provide technical support to the projects team on QC activities for new projects. You will collaborate with global QC and MSAT to ensure method validation, transfer, and qualification are completed, and contribute to lifecycle readiness of QC processes.

The role requires 4–6 years in QC or analytical labs, GMP knowledge, and strong English communication in a fast‑paced biopharma environment. Singapore‑based, on‑site in Tuas.

Qualifications

• Bachelor’s degree in chemistry, biochemistry, microbiology, life sciences or a related discipline.
• Minimum 4 to 6 years’ experience in a QC or analytical laboratory, preferably in pharmaceutical or life sciences settings.
• Practical knowledge of GMP principles and laboratory quality systems.
• Hands‑on experience with analytical methods and laboratory investigations.
• Experience coordinating method validation, verification or transfer activities.
• Good written and verbal communication skills in English.

Responsibilities

• Leads method validation, development, verification, transfer and new equipment/technology introduction.
• Provides expertise and consultation to projects team on technical QC matters to ensure compliance to applicable corporate, regulatory and external agency regulations.
• Ensures timely implementation of the projects with full compliance to corporate, regulatory and external agency regulations if applicable.
• Keeps up-to-date on regulations/development of biopharmaceutical QC method/technology to maximize digitalization, automation and robotics.
• Collaborates with global QC networks on test method innovation/evaluation to support facility design/modification for QC operations.
• Writes/reviews change controls, events/deviations, CAPAs and GMP documents (SOPs, protocols, reports).
• Ensures spendings are within project target budget.
• Performs testing when required to adhere to test release and project plan.
• Respects all safety and security policies, laboratory policies and SEHSS on site.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Lean Management

Problem Solving

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Education

Bachelor’s degree in chemistry, biochemistry, microbiology, life sciences or related

MSc in a relevant scientific discipline

Tools

Laboratory equipment qualification

Calibration programs

Computerized systems

Job description

GSK Tuas Vaccines is seeking a QC Specialist to provide technical support to the projects team on QC activities for new projects. You will collaborate with global QC and MSAT to ensure method validation, transfer, and qualification are completed, and contribute to lifecycle readiness of QC processes.

The role requires 4–6 years in QC or analytical labs, GMP knowledge, and strong English communication in a fast‑paced biopharma environment. Singapore‑based, on‑site in Tuas.