Description
We are seeking a QC Specialist to provide technical support for Quality Control (QC) related activities for new projects introduced in GSK Tuas Vaccines. The successful candidate will represent the Tuas QC unit and collaborate with global QC and global Manufacturing Science and Technology (MSAT) in all areas of QC validation and operation.
The QC Specialist will ensure that all aspects of QC testing of new projects, test method validation, analytical equipment qualification, analytical method transfer, laboratory and analytical capacity are successfully completed. The role involves leading key activities such as method validation, development, verification, transfer, and new equipment/technology introduction.
Responsibilities:
- Lead method validation, development, verification, transfer, and new equipment/technology introduction
- Provide expertise and consultation to projects team on technical QC matters
- Ensure timely implementation of projects with full compliance to corporate, regulatory, and external agency regulations
- Collaborate with global/local QC stakeholders to develop and endorse plans
- Write/review change controls, events/deviations, CAPAs, and GMP documents
- Ensure spendings are within project target budget
- Perform testing when required
Requirements:
- Bachelor's degree in chemistry, biochemistry, microbiology, life sciences, or a related discipline
- Minimum 4-6 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
Benefits:
- Competitive salary
- Opportunity to work with a global biopharma company
- Collaborative and dynamic work environment