QC Validation Lead for Pharma Projects

GSK

Singapore

On-site

SGD 70,000 - 100,000

Full time

7 days ago
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Job summary

GSK Singapore Tuas Vaccines is seeking a QC Specialist to provide technical support to the projects team for QC activities on new projects. You will lead method validation, transfer and equipment introduction, ensuring regulatory compliance and efficient project execution.

The role involves collaboration with global QC and MSAT, participation in validation master plans, and driving knowledge transfer to routine testing teams while adhering to GMP standards.

Qualifications

  • 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. Performs testing for project related activities as required.
  • 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 ensure the project maximizes the use of digitalization, automation and robotics.
  • Works closely with global/local QC stakeholders to develop and endorse Analytical transfer plan and Validation master plan, cost management and training plan
  • Collaborates closely with global QC networks on test method innovation/ evaluation to support the project team in facility design / modification, specifically for QC operations.
  • Writes/ reviews change controls, events/ deviations, CAPAs and GMP documents (e.g. SOP, protocols, reports).
  • Ensures spendings are within project target budget.
  • Perform testing when required to adhere to test release and project plan
  • Respects all safety and security polices, laboratory policies and practices on site and ensures policies and SEHSS are deployed and respected.

Skills

Data Integrity
Detail-Oriented
Digital Fluency
GxP Regulations
Lean Management
Problem Solving
Quality Assurance (QA)
Quality Control (QC)
Risk Awareness
Testing Operations

Education

Bachelor’s degree in chemistry, biochemistry, microbiology, life sciences or a related discipline
Advanced degree (MSc) in a relevant scientific discipline

Tools

Laboratory equipment qualification
Calibration programs
Computerized systems

Job description

GSK Singapore Tuas Vaccines is seeking a QC Specialist to provide technical support to the projects team for QC activities on new projects. You will lead method validation, transfer and equipment introduction, ensuring regulatory compliance and efficient project execution.

The role involves collaboration with global QC and MSAT, participation in validation master plans, and driving knowledge transfer to routine testing teams while adhering to GMP standards.

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