We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance.

Our network of 33 medicines and vaccines manufacturing sites delivered 1.64 billion packs of medicines and 389 million vaccine doses in 2025 to help make a positive impact on the health of millions of people.

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Ahead together with tailored training and career development

Start your career by helping deliver medicines and vaccines to patients around the world.

On our two-year Global Supply Chain Graduate Programme, you'll apply your scientific, engineering or digital knowledge to real manufacturing challenges while developing through rotations, training and mentoring.

What You'll Experience

• Cross-Functional Exposure: Spend time at your home site, working on cross-functional projects and rotations to deepen your expertise and knowledge of the business.
• Kaizen Assignment: A short-term breadth assignment, which could include global-focused opportunities, to expand your skills and experience beyond your home site.
• Tailored Training: Benefit from role-specific training and development, supported by a generous training budget and access to enriching resources.
• Professional & Personal Growth: Thrive in a challenging yet supportive environment, where you'll develop technical expertise through valuable on-the-job experience.

Key Programme Features

• Digital Data & Analytics (DDA) Objective: Each rotation has a DDA focus, reflecting GSK's commitment to innovation and continuous improvement, helping you to advance pharmaceutical manufacturing processes.
• Sustainability Element: Contribute to GSK's Net Carbon Zero mission by working on impactful projects that promote environmental sustainability.
• Mentoring & Networking: Build your professional network and enhance visibility through direct access to senior leaders and mentors who will guide and support your career development.

What will you do?

• Protect Patient Safety Through Science: Play a critical role in ensuring medicines meet the highest quality standards, helping deliver safe and effective treatments to patients worldwide.
• Understand the Full Product Lifecycle: Gain insight into how raw materials, intermediates, and active pharmaceutical ingredients (APIs) are tested and controlled throughout the manufacturing journey.
• Develop Expertise in Quality & Compliance: Build a strong foundation in GMP (Good Manufacturing Practice), regulatory requirements, and quality systems that are essential to the pharmaceutical industry.
• Master Analytical Science Techniques: Contribute to the development, optimisation, validation, and transfer of analytical methods used to support product quality and manufacturing performance.
• Gain Hands-On Quality Systems Experience: Work with deviations, investigations, CAPAs (Corrective and Preventative Actions), change controls, data integrity, and quality documentation, developing skills highly valued across the industry.
• Solve Complex Scientific Challenges: Use data, scientific thinking, and risk-based decision making to investigate issues, identify root causes, and deliver meaningful improvements.
• Work with Advanced Laboratory Technologies: Explore cutting-edge analytical tools and testing methodologies while helping implement new technologies and ways of working.
• Collaborate Across a Global Organisation: Partner with experts in Manufacturing, Quality, Technical Services, Supply Chain, and R&D, gaining broad exposure to how medicines are developed, manufactured, and supplied around the world.

What are we looking for?

• Technical Aptitude: Interest in science, quality and pharmaceutical manufacturing, and willingness to learn how the work supports patients.
• Continuous Improvement Mindset: A focus on growth, innovation with the ability to simplify complex processes, and apply innovative thinking.
• Communication and Collaboration: Explains information clearly, listens to others and adapts communication for the audience.
• Problem-Solving Skills: Works accurately using agreed checks and applies structured problem-solving methods.
• Priority Management: Able to manage changing priorities, with clear goals, appropriate support and agreed deadlines.
• Ownership and Support: Takes ownership of agreed tasks, asks questions and seeks support when needed.
• Adaptability: Responds constructively when priorities change and seeks support or clarification when needed.

What do we offer you?

• A competitive salary.
• Annual bonus based on company performance.
• Transport to and from site to MRT stations in centralised locations all across Singapore.
• Access to robust healthcare and well-being programmes, time off and childcare support.
• Employee recognition programmes, which reward exceptional achievements.
• Access to LinkedIn Learning and a wide range of digital learning resources to support your professional development.
• Two paid volunteering days per year, called 'Together Days'.
• Employee Assistance Programme (EAP): Free, confidential helpline and website available 24/7.
• Access to Thrive Global: A well-being platform to reduce stress, increase focus, and build resilience.

Job Data by YubHub.

Key Responsibilities:

• Draft, compile, review and update laboratory documents such as analytical methods and specifications, method validation/equivalency protocols/reports, local procedures and guidelines relating to GMP and operational framework of the laboratory
• Ensure that all data supporting the resolution of process and method issues have sufficient accuracy to allow for the correct actions to be taken to address the issue
• Contribute to the formulation and development of plans for the implementation of new or improved testing technologies and/or methods for products and/or cleaning processes
• Ensure a safe working environment for the laboratory through participating or issuing safety risk assessments for product-specific methods, techniques or materials and performing 6S inspections
• Lead or participate in investigations arising from laboratory investigations, incidents and accurately assess the impact of the failure to make appropriate recommendations for remedial or CAPA actions for follow-up

Knowledge, Skills & Experience:

• Open to fresh graduates with a minimum degree in chemistry or related field
• Minimum 3 years experience in an analytical environment, preferably in the pharmaceutical or regulated industry
• Good knowledge of GMP
• Understanding of product specification and method analysis
• Knowledge of laboratory instrumentation
• Laboratory support procedures
• Regulatory requirements for method validation
• Good communication skills
• Problem-solving skills
• Project management skills

Job Data by YubHub.

The successful candidate will ensure that all site utilities, water, environmental monitoring, and product testing activities are properly analysed and executed, and the results recorded in full compliance with current Good Manufacturing Practice (cGMP) and regulatory requirements that meet the defined quality standards.

Key Responsibilities

• Ensures that all water, environmental monitoring, site utilities and product testing samples are analysed and tested according to the stipulated quality requirements so as to provide accurate test results for correct usage decisions.
• Develops a strategy for the site with respect to environmental monitoring and water systems.
• Performs microbiological risk assessment for all non-sterile products.
• Ensures that external service providers and suppliers for microbiology laboratory are managed in accordance to GSK requirements.
• Ensures regulatory compliance, performs L1 audit and supports L2/L3/L4 audit as Microbiology Subject Matter Expert (SME).
• Leads or participates in investigations arising from micro-related and utilities investigations, incidents and accurately assesses the impact of the failure so as to make appropriate recommendations on remedial actions for follow-up.
• Works with the relevant R&D groups to support micro-related activities and micro-risk assessment for New Product Introduction, ensuring that the activities are carried out in accordance to the required standards and procedures.
• Works closely with external staff and at-line level to enable the localization and transfer of technology / knowledge / methodologies into standard order fulfillment activities.

Requirements

• Minimum degree in Microbiology or Life Sciences.
• Minimum 3-5 years' experience in an analytical environment, preferably in the pharmaceutical industry.
• Good knowledge of GMP.
• Basic knowledge and on-going awareness of regulatory requirements (includes safety) on controlled environment and water system.
• Very good knowledge of microbiological test methods.
• Good knowledge of manufacturing processes and plant layouts of GlaxoSmithKline Manufacturing.
• Good communication skills.
• Basic financial management skills.
• Basic knowledge of business process within GSK.
• People Management skills.

Job Data by YubHub.

As a trainee, you will go through a 15-month structured on-the-job training programme with GSK, gaining hands-on experience, industry-relevant skills, and mentorship from experienced professionals in a world-leading biopharmaceutical environment.

Role Description: This position reports to the Production Superintendent in our Value Streams (VS 1, 2 or 3) team and is an integral member of Production Shift Team. GSK is committed to an employee-orientated, high performance culture that emphasises process automation, quality compliance and continuous improvement.

Responsibilities:

• Execute key process operations in accordance to established batch instructions and schedule to make APIs and intermediates as well as plant changeover
• Learn Process and Workplace Safety and cGMP knowledge for manufacturing and demonstrate understanding during execution
• Identify opportunities for improvements and carry out short-term improvement projects to achieve benefits
• Inspect and maintain house-keeping of assigned area for clean and safe working conditions
• Perform plant troubleshooting using problem-solving tools to minimise plant stoppages and safety or quality incidents

Education / Qualification:

• NITEC, Higher NITEC or Diploma in Chemical Process / Technology / Engineering related

What you will learn:

• Foundational on-the-job training experience working in cGMP and key Global Supply API manufacturing site with state-of-the-art manufacturing facilities
• Training to be an advocate for Continuous Improvement, with introductory basics on Lean Sigma concepts and coaching by supervisors
• Ability and willingness to work on 12-hour shift operations

Benefits:

• Monthly training allowance including shift allowances
• On-the-job training with a diversified team of professionals
• Employee benefits including medical and insurance coverage, leave entitlements, and onsite cafeteria benefits
• Transport to and from site to MRT stations in centralised locations across Singapore

Job Data by YubHub.