Site Engineering Lead at GSK

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 lead site engineering, maintenance, and technical teams to keep our manufacturing site safe, compliant, and reliable. You will work closely with operations, quality, EHS, and supply chain to deliver capital projects and continuous improvements. We value clear leaders who coach others, solve complex problems, and drive practical, measurable results. This role offers strong career growth, the chance to shape site strategy, and meaningful impact aligned 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 site engineering and maintenance programs to ensure safe, compliant and reliable production. Manage capital projects from scope through commissioning, meeting budget and schedule targets. Oversee preventive and corrective maintenance, spare parts strategy, and equipment reliability programs. Ensure engineering systems meet regulatory, quality and EHS requirements and global engineering standards. Drive energy, sustainability and continuous improvement initiatives that reduce cost and risk. Build and develop the engineering team, including contractors, and support cross-functional site priorities. 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 (Mechanical, Electrical, Chemical, Civil or related). At least 10 years of relevant engineering or maintenance experience in a regulated manufacturing environment. Minimum 2 years managing technical staff or engineering teams. Demonstrated experience delivering capital projects, including budgeting and project governance. Experience with maintenance strategies, reliability practices, and equipment lifecycle management. Demonstrated experience in the regulated manufacturing industry, including successful management and support of FDA and EMA inspections. Preferred Qualification If you have the following characteristics, it would be a plus: Advanced degree in Engineering or relevant technical discipline. Experience in pharmaceutical, biomanufacturing, or highly regulated process industries. Experience with automation, controls, and plant control systems. Proven track record in energy management, sustainability, or utility optimization. Project management certification or demonstrated program delivery experience. Strong stakeholder engagement and change leadership skills. Location and Working Model This role is based in the United States. The position may be on-site or hybrid depending on site needs. Expect regular on-site presence to support operations, projects, and the engineering team. What we offer You will join a purpose-driven organization where your work supports patient outcomes. You will find development opportunities, visible impact, and a collaborative culture that values inclusion and respect. We encourage applicants from all backgrounds and welcome people who