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.
Join Us at Zebulon
One of GSK's flagships and fastest‑growing manufacturing sites, where you'll tackle complex products, shape the future of smart manufacturing, and see your impact reach millions of patients worldwide. If you're energized by robotics, digital innovation and AI – and want to grow your career in a high‑performing, purpose‑driven environment – we'd love to hear from you.
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, 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 to 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 perform 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 delivery of 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, communication 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 Solving 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.
Key Differentiators About GSK and Zebulon
- Commitment to inclusion and diversity as a critical advantage.
- Focus on cultivating a positive work environment that cares for employees.
- Demonstrated opportunities for continued career growth driven by individual ambition.
- Leaders that care about team growth and company growth.
- Priority focus on Safety and Quality.
- Clean and GMP compliant work environment.
- Onsite cafeteria.
- Onsite gym.
- Temperature‑controlled facility.
- 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 site leadership. The successful candidate will be expected to spend most of their time at the manufacturing site and on project locations.
What We Offer
You will join a team that values inclusion, safety, and practical problem solving. You will be supported with learning opportunities and mentoring to grow your career. You will work on projects that matter and help deliver real‑world impact through strong engineering and collaboration.
Accommodation & Equity
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at usrecruitment.adjustments@gsk.com.
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.