Polytechnic Internship - Quality Control, Singapore (March 2027 to August 2027)

GSK

Singapore

Presencial

SGD 17 000 - 21 000

Tempo integral

Há 3 dias
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Resumo da oferta

GSK Singapore invites applications for a Quality Control Internship (2027). You will engage in document management, QC data handling, and hands-on lab work including reagent prep and testing, while upholding 6S and safety standards.

The role offers exposure to GMP/GDP practices and cross-functional collaboration with global scientists. The six-month program runs from March 2027 to August 2027, with rolling applications and an emphasis on building practical QA/QC skills for students enrolled in

Qualificações

  • Diploma from an accredited polytechnic in the specified disciplines.
  • Enrollment in a local polytechnic for the duration of the internship with a credit-bearing arrangement.
  • Proficiency in English, both written and spoken.

Responsabilidades

  • Manage and archive documents; log and summarize materials.
  • Understand WoWs in QC and perform data tabulation.
  • Conduct QC operations including logistics, reagent prep, EM sampling and testing.
  • Maintain 6S and good housekeeping; ensure QC material inventory.
  • Support area continuous improvement and adhere to safety policies.

Conhecimentos

Data Integrity
Detail-Oriented
Digital Fluency
GxP Regulations
Lean Management
Problem Solving
Quality Assurance (QA)
Quality Control (QC)
Risk Awareness
Testing Operations

Formação académica

Diploma in Pharmaceutical Sciences / Applied Science / Chemical Engineering

Ferramentas

SAP
LES

Descrição da oferta de emprego

Help us get ahead of disease together with our Quality Control Internship, 2027:

Education required: Diploma from an accredited polytechnic preferably in Pharmaceutical Sciences/Applied Science/Chemical Engineer discipline

Other requirements: Must be enrolled at local polytechnic for the duration of your internship and doing a credit bearing internship

Language requirement: Written and spoken fluency in English

Internship period : March 2027 to August 2027

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?

What will you do?
  • Management of documents (e.g. Proper archival of documents, summarize and tabulate documents in specific logs).
  • Understand WoWs in QC
  • Data tubulation
  • Perform QC operations such as logistics, reagent preparation, EM sampling, and testing in laboratory
  • Performs 6S and good housekeeping of work area
  • Ensures good inventory of QC materials
  • Area continuous improvement
  • Adhere to all safety and security policies and practices
What will you learn?
  • Acquire Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) knowledges
  • Gain knowledge in GMP and Safety audit preparation
  • Requirement around document archival
  • Material flow from receipt, testing to disposal
  • Usage of laboratory systems such as SAP, LES
  • Understand how data generated in quality control is used in GMP environment
  • Various laboratory techniques
  • Gain exposure with possibility to participate/support ad-hoc site and QC activities.
What are we looking for?
  • A lively interest in quality control, the commercial world and the biopharma industry
  • Appetite to work as team in quality control, building strong relationships with key stakeholders
  • Meticulous, organized, logical and self-motivated
  • 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
  • Good ability to prioritize tasks assigned.
  • Experience in the use of Microsoft Office
What do we offer you?
  • Understand and experience the GSK Culture
  • Work with a diversified team of scientists across the globe
  • 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
Skills
  • Data Integrity
  • Detail-Oriented
  • Digital Fluency
  • GxP Regulations
  • Lean Management
  • Problem Solving
  • Quality Assurance (QA)
  • Quality Control (QC)
  • Risk Awareness
  • Testing Operations
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.

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