Value Stream Engineer I

Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.<br>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.<br>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 provide technical and process support to a Value Stream team in our Singapore manufacturing site. You will work with manufacturing, quality, and technical teams to solve problems, improve processes, and support safe, compliant production. We value curious problem-solvers who communicate clearly, act with integrity, and seek practical improvements. This role offers clear growth paths, hands-on impact on manufacturing performance, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead investigations of process deviations and support corrective and preventive actions to close root causes. - Support production teams with process monitoring, batch record reviews, and quality risk assessments. - Plan and execute process improvement initiatives, including batch record and alarms improvements. - Support validation activities, trials, and technical transfer to enable new or changed processes. - Prepare clear technical documents and deliver training to operators and stakeholders. - Work with cross-functional teams to plan and deliver project deliverables on time and in scope. Responsibilities - Manage complex deviation investigations and guide CAPA implementation. - Monitor process parameters and report trends to the Quality Review Board and stakeholders. - Perform gap analysis against quality systems and support remediation actions. - Drive small to medium improvement projects using data-driven tools. - Coordinate resources and contractors when required to deliver maintenance, trials or transfer activities. - Communicate progress and risks promptly to manufacturing and quality teams. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Bachelor’s degree in engineering, science or related discipline. - At least 1 year of experience in a regulated manufacturing environment. Pharmaceutical or biotech experience preferred. - Strong troubleshooting and problem-solving skills with practical, evidence-based thinking. - Clear written and verbal communication skills suitable for cross-functional work. - Basic project management skills and ability to coordinate tasks and resources. - Comfortable working on-site at our Singapore manufacturing facility (this role is on-site). Preferred Qualification If you have the following characteristics, it would be a plus - 3 or more years of experience in pharmaceutical, biotech, or chemical manufacturing. - Experience with validation, technical transfer or commissioning activities. - Familiarity with continuous improvement methods such as Lean or Six Sigma. - Experience working with batch records, process control systems, or alarms management. - Knowledge of cGMP, quality systems, and risk assessment methods. - Ability to coach and influence operators and colleagues to adopt improvements. How to apply We welcome applicants from all backgrounds and experiences. If this role matches your skills and ambitions, please apply. Tell us how your experience will help our manufacturing teams improve quality, safety and reliability. We look forward to learning about you.<p></p><p><b>Why GSK?</b></p><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><p> </p><p>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.</p><p> </p><p>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.</p><p></p><p>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 <a target="_blank" href="mailto:APACRecruitment.Adjustments&#64;gsk.com"><span style="color:#0000ff"><u>APACRecruitment.Adjustments&#64;gsk.com</u></span></a>. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.</p><p></p><p><b>Important notice to Employment businesses/ Agencies</b></p><p>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&#39;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.</p>