Senior Biotechnologist 1

Job description

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 join our Singapore manufacturing team to support the set-up and steady-state operation of end-to-end bioprocess production. You will work closely with colleagues in operations, quality and engineering to run safe, reliable and compliant manufacturing processes. We value hands-on people who are curious, safety-minded and ready to learn. This role offers clear technical growth, visible impact on supply, and the chance to help unite science, technology and talent to get ahead of disease together. 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 monitor bioprocess equipment and systems, including media and buffer preparation, fermentation, purification and filtration, following established procedures. - Support commissioning, installation and qualification activities to meet project milestones and support new equipment introductions. - Maintain accurate production and quality records and support timely batch handovers and electronic record systems. - Follow good manufacturing practice and site safety rules; report deviations and support investigations and corrective actions. - Coach and support colleagues through on-the-job training and knowledge transfer activities. - Identify and suggest practical process or equipment improvements to increase safety, quality and uptime. Why You? Working pattern This role is on-site at our Singapore manufacturing facility. Shift work and occasional on-call duties may be required. You will collaborate regularly with colleagues across operations, quality and engineering. The role gives strong development opportunities and exposure to commissioning projects and continuous improvement work. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Right to work in Singapore and willingness to work on-site at a manufacturing facility. - Diploma, Higher Nitec or equivalent practical experience in biotechnology, chemical engineering, life sciences or a related field. - At least 2 years practical experience in manufacturing, process or laboratory operations in a regulated or technical environment. - Demonstrable ability to follow procedures, complete accurate documentation and work to quality standards. - Strong awareness of safety, hygiene and environmental requirements and ability to apply them consistently. - Good communication skills in English and ability to work collaboratively with different teams. Preferred Qualification If you have the following characteristics, it would be a plus - Experience with biologics or chemical manufacturing activities such as media/buffer prep, fermentation, chromatography, filtration or ultrafiltration. - Experience participating in commissioning and qualification activities (for example, IQ/OQ/PQ). - Familiarity with computerized production systems, MES or electronic batch records. - Practical troubleshooting skills for process or mechanical equipment and ability to lead investigations. - Experience developing or improving standard operating procedures, checklists or training materials. - Prior experience coaching or leading small teams and supporting knowledge transfer. What we value We welcome applicants from different backgrounds and experiences. We are committed to inclusion and to creating a workplace where everyone can do their best work. If you do not meet every preferred qualification but bring practical skills, motivation and a willingness to learn, we encourage you to apply. Ready to apply? If this role feels like the right next step, please apply. Join us to grow your skills, make a visible impact and help unite science, technology and talent to get ahead of disease together. We look forward to hearing from you. Skills Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Processes, Problem Solving, Production Management, Quality Compliance, Regulatory Compliance, Risk Awareness 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.