About the role
AI summarisedThis is a 15-month structured on-the-job training program (Attach-and-Train) designed to build the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry within GSK. This program is specifically for Singapore Citizens and Permanent Residents.
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 proficiency.
- Must be a Singapore Citizen or Permanent Resident.
- Ability to work on-site in Singapore.