Polytechnic Internship - Quality Control (Systems & Support), Singapore (Ma at GSK

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

09 Feb, 26

Salary

0.0

Posted On

12 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Good Manufacturing Practices, Good Documentation Practices, Microsoft Office, Organized, Self-Motivated, Adaptability, Prioritization

Industry

Pharmaceutical Manufacturing

Description

Help us get ahead of disease together with our Vaccines Business Area / Quality Control (QC) Internship, 2026: Education required: Current student enrolled in a Diploma from a local polytechnic, preferably in Biologics / Chemical & Process Technology / Chemical & Pharmaceutical Technology / Pharmaceutical Science Other requirements: Must be enrolled at a Singapore local polytechnic for the duration of your internship & doing a full-time credit bearing internship Language requirement: Written and spoken fluency in English Internship period: March to August 2026 Application deadline: As applications will be reviewed on a rolling basis, we recommend applying as soon as possible for your application to be considered. This vacancy will be closed once we have enough applications for consideration. Are you looking to gain valuable world work experience and help to positively impact the health of billions of people? Apply for a GSK Internship today! 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? You will discover about the different processes in the QC department (E.g. Systems & Support, Chemistry & Biology lab) You will manage documents within the QC department (E.g.To ensure proper archival of documents, summarize and tabulate documents in specific logs) You will support the QC Systems & Support team for required activities which you will be trained in You will perform data tubulation and trending of data collected for QC tests for the QC Laboratory Execution System (LES) You will be involved in continuous improvement actions for the QC department You will gain insights to on-site Regulatory Audits (if available) You will gain exposure with possibility to participate/support ad-hoc site and QC activities What will you learn? Acquire in depth knowledge on Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) knowledge Be familiar with different QC functions Gain knowledge in GMP and Safety audit preparation Documentation flow from creation to archival process Material flow from receipt, testing to disposal What are we looking for? Basic Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) knowledge Experience in the use of Microsoft Office Meticulous, organized, logical and self-motivated Adaptability to change and working under pressure Good ability to prioritize on tasks assigned 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 Apply and develop soft skills such as interpersonal, communications and negotiation skills Transport to and from site to MRT stations in centralised locations all across Singapore Let’s do this! You’ll find hints, tips and guidance on our recruitment process on our website. Learn more about the application process: gsk.to/ETprocess Hear more from our past interns here: GSK Internship Experience Get some tips from our interns: Top Tips from Our Interns You can learn more about GSK and our careers here https://www.gsk.com/en-gb/careers/ Apply now! Need help with your application? Please email us at apac.earlycareers@gsk.com and let us know how we can help you. #GSKSingapore #EarlyCareers #SGInternships Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. We are a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Find out more on our career site.

Responsibilities

You will discover different processes in the QC department and manage documents within the QC department. You will support the QC Systems & Support team and perform data tabulation and trending of data collected for QC tests.