Polytechnic Internship - Quality Control (Microbiology & Services), Singapo at GSK

Genarp, Skåne County, Sweden -

Full Time

Start Date

Immediate

Expiry Date

21 Jul, 26

Salary

0.0

Posted On

22 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Microbiology, Quality control, Laboratory operations, Data tabulation, Lean process improvement, Inventory management, GMP compliance, Document archival, SAP, Laboratory execution system, Project management, Problem-solving, Communication, Teamwork, Safety compliance

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 Pharmaceutical Sciences, Applied Science or Chemical Engineering 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/December 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? Management of documents and data tabulation Understand WoWs in laboratory May be required to perform lab operations such as reagent preparation, sampling on production floor, and testing in laboratory Learns about lean process improvement tools and performs good housekeeping of laboratory, work area and equipment Ensures good inventory of QC materials Involved in area continuous improvement Adhere to all safety and security policies and practices What will you learn? Requirement around document archival Usage of laboratory system such as Systems, Applications & Products (SAP) and Laboratory Execution System (LES) Understand how data generated in laboratory is used in GMP environment Various laboratory techniques What are we looking for? An individual who is interested in learning more about a manufacturing environment and vaccines A lively interest in laboratory work, the commercial world and the biopharma industry Appetite to work as team in the laboratory field, building strong relationships with key stakeholders Adaptability to change and working under pressure Excellent communication skills that help you influence Strong problem-solving skills driven by curiosity Drive and confidence to trust your own judgment Great project management skills and the ability to prioritize 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: 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 #SGInternship #EarlyCareers 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. We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels. 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.

Responsibilities

The intern will manage laboratory documentation, perform data tabulation, and assist with reagent preparation and sampling on the production floor. They will also participate in lean process improvement initiatives and ensure proper inventory management of quality control materials.