Capital Project Engineer

Position Summary You will support the delivery of capital projects within the SE Capital Project Team involving small to medium complexity facilities and/or production equipment or systems, ensuring that all outcomes meet the defined project objectives for cost, schedule, quality, and safety, while delivering the intended business benefits. Responsibilities Plan and manage multiple facility and equipment projects simultaneously that are of small to medium complexity within a GMP production environment, ensuring adherence to the GSK Project Management Framework (PMF). For higher complexity projects, support the assigned Project Manager by providing your assistance to ensure successful project delivery. Plan and develop a robust technical project scope or solution, manage and drive project team accountability, oversee project costs and schedule, mitigate risks, and monitor and control the project according to the GSK PMF. Ensure projects are delivered within the approved budget, on schedule, and to the defined scope, while maintaining high standards of safety and quality. Oversee the entire capital project life cycle, from initial project scope definition and funding requests through to project execution, qualification, startup/turnover, and asset capitalization. Recognize the roles, responsibilities, and expertise of other specialists within the organization, engaging them as needed to develop comprehensive technical designs and enhance project outcomes. Coordinate and meticulously plan and control all elements of the project schedule, ensuring timely and effective project delivery. Ensure that project design and delivery comply with all relevant EHS and Engineering and Quality procedures/standards, leveraging the expertise of SMEs to confirm compliance throughout the project lifecycle. Develop a comprehensive construction plan with appropriate permits and risk assessments, ensuring safe execution and performing routine safety and quality confirmations with other experts. Maintain clear and effective communication regarding all aspects of the project, both verbally and in writing, including the delivery of presentations to stakeholders. Maintain and organize project deliverables in a structured file system that demonstrates adherence to PMF, safety, and compliance requirements. Basic Qualifications Bachelor’s degree in engineering (mechanical, chemical, electrical, civil, or related field). 5+ years of experience in capital project engineering in manufacturing, process, or utilities environments. Solid experience in a manufacturing environment with hands‑on experience delivering production equipment and/or facility equipment changes. Experience managing project deliverables, schedules, and budgets. Authorization to work in the United States without company sponsorship. Preferred Qualifications Professional Engineer (PE) license or equivalent certification. Experience with pharmaceutical or life sciences manufacturing facilities. Familiarity with process control systems, utilities, and clean utilities design. Experience with project management tools and project cost control systems. Experience supporting commissioning, qualification, and validation activities. Experience working on projects that required regulatory or environmental permitting. Strong knowledge of engineering design, construction practices, and codes. Effective communicator with experience working in cross‑functional teams and with contractors. The ability to plan effectively and deliver sustainable small to medium CapEx projects. Ability to work well under pressure with tight timelines. Excellent consultative, listening, communications and analytical skills. Must be flexible, adaptable and a team player. Negotiation and conflict resolution skills and ability to motivate highly skilled and trained individuals. Must be proficient with MS Word, Excel, PowerPoint, and Project. Personal Effectiveness: Customer Focus, Decision Making, Influencing. GPS Level / Problem Solvent certifications desirable. About the Zebulon Site GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount and Wake Forest. Benefits Commitment to inclusion, valuing diversity as a critical advantage. Focus on cultivating a positive work environment that cares for employees. Opportunities for continued career growth driven by individual ambition. Leadership that cares about teams and growth of individuals and the company. Priority focus on Safety and Quality. Clean and GMP compliant work environment. Onsite cafeteria. Onsite gym. Temperature‑controlled environment. Licensed onsite Health & Wellness clinic. Working Arrangement This role is on‑site at our United States facility with some flexibility for hybrid collaboration when approved by the site leadership. The successful candidate will be expected to spend most of their time at the manufacturing site and on project locations. Equal Employment Opportunity GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. For assistance with accommodations or other aid required to apply for a job at GSK, contact us at View email address on click.appcast.io. #J-18808-Ljbffr GlaxoSmithKline