Quality Systems & Data Manager

GSK•Zebulon, NC

8d•Hybrid

About The Position

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 and strengthen quality systems that support safe, compliant and reliable manufacturing and laboratory operations. You will work closely with site teams, technical experts and external partners to maintain strong processes and clear data. We value practical quality systems experience, calm decision-making and a collaborative approach. This role offers growth, visible impact on patient supply and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Requirements

Bachelor’s Degree in a Scientific, Technical, Computer Science discipline or equivalent experience
8+ years’ experience in commercial pharmaceutical manufacturing facility. , biotech or related regulated quality operations, including supervisory roles.
Hands-on experience: change control, deviation investigations, CAPA, document control, and validation or qualification activities.
Familiarity with digital tools and systems.

Nice To Haves

Advanced degree in fields such as Chemistry, Biology, Pharmacy, or Engineering.
Experience managing supplier or contract manufacturing quality relationships.
Knowledge of electronic quality management systems, data integrity frameworks, and regulatory expectations.
Expertise in continuous improvement, data analytics, lean six sigma, and industry standards (cGMP, ISO).
Leadership experience, strong collaboration skills, and effective decision-making capabilities.

Responsibilities

Responsible for creating and driving the Quality digital strategy in collaboration with site and central functions, including delivery of smart manufacturing initiatives.
Provide leadership and strategy for the site data integrity and governance program.
Uses lean six sigma methodologies to advance systemic quality improvements through the GSK production system.
Ensure comprehensive training compliance for all relevant personnel, maintaining up-to-date training records and facilitating necessary training programs.
Manages implementation of local updates to site quality digital systems including VQMS, MERP through appropriate change management procedures.
Develop, implement, and monitor the Quality Improvement Plan, and drive continuous improvement initiatives.
Collaborate with cross-functional teams to ensure alignment and integration of quality systems and processes.
Develop and maintain quality documentation systems, ensuring regulatory compliance, accessibility, and continuous improvement.
Drive initiatives for Quality Culture at site.