Internship - QA for Quality Control and Materials Management, Singapore (July to December 2025)

**Help us get ahead of disease together with our Vaccines Business Area / Quality Assurance (QA) for Quality Control and Materials Management** **Internship, 2025**:
**Education required**:Undergraduate studying a Bachelor’s Degree from an accredited college/university, preferably in Faculty of Science (Life Sciences, Chemistry, Pharmacy & Pharmaceutical Science) or Faculty of Engineering (Biomedical Engineering, Pharmaceutical Engineering, Chemical Engineering)

**Other requirements**: Must be enrolled at a SG university for the duration of your internship and doing a credit-bearing internship

**Language requirement**: Written and spoken fluency in English

**Internship period**: July to December 2025

**Application deadline**: 31 January 2025

A GSK internship offers you the opportunity to kickstart your career - to take on a real role with genuine impact You’ll take on challenging, serious work on live projects or assignments. You’ll also get to learn from us, develop your skills and gain valuable experience for wherever the future takes you.

With an investment of S$510 million, our state-of-the-art vaccines manufacturing facility at Tuas was opened in June 2009 by Singapore's Prime Minister Lee Hsien Loong, coinciding with our 50th anniversary in Singapore. Comprising two production buildings, an administration block, quality control laboratories, utility plant and warehousing, the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.

Tuas is a key manufacturing site within our network supplying the active ingredient used to make our pneumococcal conjugate vaccine. This paediatric vaccine is indicated for the active immunisation against pneumonia, invasive diseases and acute otitis media caused by _Streptococcus pneumoniae_ in infants and children.

Tuas site also focuses on manufacturing Hib (_Haemophilus influenzae type b_) antigen which is used in the manufacture of several paediatric vaccines. Hib is a bacterium responsible for invasive diseases, such as severe pneumonia and meningitis, contracted almost exclusively by children less than five years old.

These two vaccine products manufactured at Tuas cover a number of diseases causing paediatric mortality in the world, making a significant contribution to our global health agenda. The site continues to invest in developing technical capability and process improvement, and embracing new technology such as digital, data and analytics to position itself as a centre of excellence for the manufacture of vaccines.

**What will you do?**

We are looking to provide a learning opportunity for an intern in supporting quality oversight activities for Quality Control (QC) and/or Incoming Material (IM) activities. The intern will work under the supervision of the QA manager / lead to deliver projects related to simplification of existing workflow while supporting the day-to-day manufacturing and testing operations. The intern will get the opportunity to collaborate with a wide array of functions (QC, Supply Chain, Technical) and appreciate how to ensure smooth operations of a biopharmaceutical manufacturing plant.

As an intern, you will:

- Support day-to-day oversight of Quality Control (QC) and Incoming Material (IM) activities
- Support projects related to existing workflow simplification
- Perform timely management of documentation
- Drive continuous improvement mindset

**What will you learn?**
- Current Good Manufacturing Practices (cGMP) in biopharmaceutical manufacturing environment
- General understanding on biopharmaceutical manufacturing processes
- Basic project management skills

**What are we looking for?**
- A keen interest in consumer healthcare science, product and development, and a passion for knowledge
- Proficient in use of IT and software/systems
- Knowledge of Current Good Laboratory Practices (cGLP) & Current Good Manufacturing Practices (cGMP)
- Possesses common laboratory techniques
- Laboratory experience in the pharmaceutical industry
- Able to demonstrate ability to take initiative, think and work independently, and problem-solve
- Good scientific English writing and oral communication skills
- Deadline-driven, flexible with self-reliance to work in an empowered environment
- Awareness and ability to work within culturally diverse teams
- Strong drive for performance and attention to details
- Proficient use of Microsoft tools (e.g., Word, Excel, Power Point)
- Knowledge of Microsoft Power Platforms (Apps, Automate, BI) will be a plus

**What do we offer you?**
- Understand and experience the GSK Culture
- Work with a diversified team of professionals
- Implement technical knowledge and skills that you have acquired at school
- Transport to and from site to MRT stations in centralised locations across Singapore

**Let’s do this**

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