About the role
AI summarisedEntry-level 15-month attach-and-train programme at GSK Singapore focused on Quality Assurance operations for biopharmaceutical manufacturing. Trainee will handle incoming material review, documentation, investigations, and quality metrics while receiving structured on-the-job training.
BiopharmaOnsiteQuality
Key Responsibilities
- Support incoming materials review and release activities
- Maintain and update quality documentation and records in line with good documentation practice
- Assist in investigations, root cause analysis and corrective and preventive actions
- Help manage third party change notifications to assess for any risks
- Liaise with internal teams and third-party partners on quality queries and follow up on actions
- Contribute to routine quality metrics, trend reports and simple improvement projects
Requirements
- Bachelor’s degree in pharmacy, life sciences, chemistry, engineering or a related field
- 0 to 2 years’ experience in a manufacturing, laboratory, quality or supply role
- Basic knowledge of good manufacturing practices and quality systems
- Strong attention to detail and good record-keeping discipline
- Clear written and spoken English
- Singapore Citizen or Permanent Resident