Vice President Sterility Assurance

Vice President, Sterility AssuranceOur global supply chain is critical to manufacturing and supplying reliable, high-quality medicines and vaccines to meet patients needs and drive our performance. It includes 37 medicines and vaccines manufacturing sites which help to make a positive impact on the health of millions of people.Supply chain teams are part of how we prevent and change the course of disease, bringing our innovations to patients as quickly, efficiently and effectively as possible. They're involved early in product and process development, working with R&D to make sure that what works in clinical trials can be scaled up to commercial production.Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We're using data to help us monitor production in real time, spot ways to increase yields and predict when equipment needs maintenance. We're using smart manufacturing technologies for greater efficiency, productivity, sustainability and cost savings. We can augment our human creativity, expertise and problem solving with data and AI, increasing our impact and delivering better and faster for patients.As the Vice President, Sterility Assurance, you will provide outstanding leadership in shaping and delivering a global sterility strategy across Engineering, QA, Business Units and MSAT. You will drive standardisation, implement robust risk controls, and ensure inspection readiness across GSKs network and end-to-end business processes, positively impacting quality and compliance.Key Responsibilities:Own and deploy sterility assurance strategy, standards, and governance to ensure compliance to regulatory expectations.Lead cross-functional alignment and risk mitigation across Engineering, QA, and MSAT.Ensure contamination control strategy is standardized and embedded in QMS.Oversight of facility design and equipment reliability aligned with sterility assurance requirements.Lead cleaning validation, process control, and supplier qualification as it relates to sterility assurance standards.Ensure QMS integration, deviation management, and inspection readiness.Chair monthly governance forums and drive strategic decisions.Build capability through Communities of Practice.Strategic Objectives:Accountable for transformation of sterility assurance global standards across Engineering, MSAT and Quality and ensuring that they are in use across all sites.Set vision for the future to proactively meet regulatory expectations.Accountable for program management for execution / implementation to global standards.Deliver Annex 1 compliance through standardized global policies.Implement KPI dashboards for contamination control and cleaning validation.Define clear project and governance frameworks to clarify roles and responsibilities between global and local teams.Drive continuous improvement and proactive inspection readiness.Lead the uplift in capability building and leadership development across functions.External network/advocacy with industry forums and regulators to keep pace with evolving regulatory expectations and emerging technology.Basic Qualifications:Bachelors degree in microbiology, life sciences, engineering, or related field, or equivalent experience.Significant experience in sterility assurance, microbiology, or quality in a regulated manufacturing environment.Proven leadership in cross-functional roles including QA, Engineering, and MSAT.Strong knowledge of Annex 1, GMP, and global regulatory requirements.Experience in inspection readinessExcellent communication, governance, and stakeholder management skillsPreferred Qualifications:Advanced degree in microbiology, pharmaceutical sciences, or engineering.This role can be based at one of our manufacturing sites in the US (East coast), Europe or UK.Closing date for applications: 28th November 2025