Business Introduction
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
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.
Position Summary
You will support and run key bioprocess steps to make high-quality bulk drug substance. You will work closely with operators, technical leads and quality colleagues. We value attention to detail, a safety-first mindset, and a drive to learn and improve. This role offers clear growth paths, hands-on experience with regulated processes, and the chance to contribute to work that helps people through better medicines.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Operate and complete assigned process stages, following procedures and work instructions.
- Follow cGMP, safety and environmental rules to keep people and facilities safe.
- Record batch data and complete documentation accurately and on time.
- Support investigations of process deviations and help implement corrective actions.
- Train, coach and guide new team members during on-the-job activities.
- Take part in continuous improvement, commissioning or technology transfer activities.
Why You?
This role is on-site at our Singapore biomanufacturing facility. You will join a team that supports learning and development. We welcome people who want to build technical depth and step into more responsible roles over time.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Diploma or equivalent in biotechnology, chemical technology, chemical engineering, life sciences or related discipline.
- At least 2 years’ experience in biologics, pharmaceutical, chemical or other regulated manufacturing environment.
- Practical experience working under Good Manufacturing Practice (GMP) or similar regulations.
- Familiarity with upstream or downstream operations such as fermentation, purification, buffer preparation, or isolator work.
- Clear written and verbal communication for accurate documentation and handovers.
- Comfortable working on-site in cleanroom or controlled environments and following safety procedures.
Preferred Qualification
If you have the following characteristics, it would be a plus:
- Prior experience with batch records, SOPs and deviation/CAPA processes.
- Experience training or mentoring colleagues in operational tasks.
- Basic knowledge of equipment commissioning, qualification or validation activities.
- Hands-on experience with manufacturing equipment and routine maintenance support.
- Demonstrated problem-solving in process or quality challenges.
- Willingness to work flexible shift patterns when required.
What we offer
You will gain practical bioprocess experience in a regulated setting. You will have access to development plans and learning resources. You will work with people who care about safety, quality and helping patients.
How to apply
We want to hear from you. Please submit your CV and a short cover note explaining your interest in this role and how your experience fits. If you have questions about the role or the hiring process, reach out and we will reply. We welcome applicants from all backgrounds and encourage people who care about making a difference to apply.
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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