• Oversee the strategy, delivery, and lifecycle management of Infovista’s enterprise technology roadmap, aligned with corporate objectives and growth priorities. • Ensure coherence and prioritisation across platforms, applications, data, and operations are secure, scalable, resilient, and fit for current and future product needs. • Act as principal technology advisor to the COO and ELT, providing clear, commercially grounded insight and recommendations. • Provide executive accountability for the availability, performance, and reliability of all production and internal systems. • Ensure strong operational governance, incident management, and service assurance. • Embed modern operational practices to ensure initiatives are data‑backed, and aligned with strategic priorities. • Enable teams through standardised tooling, automation, and well‑governed platform services. • Lead and develop senior technology leaders across Platforms, InfoSec and IT. • Build a high‑performing, accountable technology organisation with clear ownership and outcomes. • Foster global collaboration across technology and business leadership. • Establish clear technology governance, operating models, and decision‑making frameworks.

• Build the operational and technological DNA of a corporate group from the ground up • Define the operating model and the technological roadmap • Identify improvement opportunities • Digitize work preparation and implement automated production planning • Lead the operations team and develop employees

• Define and drive technical architecture for both our mature search platform and evolving RAG solution • Make critical technical decisions on scaling, infrastructure, and product evolution • Solve difficult technical problems that the team escalates • Guide technology choices and evaluate new tools/approaches (especially AI-assisted development) • Own deployment strategy, operational readiness, and infrastructure reliability across all engineering initiatives. • Lead and mentor a team of 6 experienced engineers (5 developers + 1 solutions engineer) • Foster a culture of technical excellence, autonomy, and continuous learning • Conduct code/design reviews and provide thoughtful technical feedback • Act as a coach rather than commander - this team values collaboration • Review and assess technical requirements in enterprise contracts • Handle security questionnaires and compliance requirements (SOC2, GDPR, etc.) • Lead our SOC 2 compliance / audits • Collaborate with CEO, product, sales and marketing leadership on product roadmap • Balance technical debt, feature development, and operational stability • Contribute to architecture and design (you don't need to write code daily, but you should be able to) • Stay current with AI/ML developments, especially in RAG and LLM applications • Champion modern development practices (we use AI-assisted tools like Claude Code, Codex)

Title: MSAT Senior Technology SME Location: Marietta PA United States You will be an experienced Manufacturing Science & Technology (MSAT) Senior Technology Subject Matter Expert (SME) in the United States. You will work across technical, quality and other partners to support commercial Drug Substance and Drug Product Vaccine manufacture with technical lifecycle ownership in your area of expertise (i.e. mixing/homogeneity, ultrafiltration/diafiltration, chromatography, formulation, aseptic filling and AVI). You will lead technical strategy, troubleshooting, manufacturing scale-up activities, process robustness initiatives and technology transfers from donor sites for new and established products. We value clear problem solvers who communicate well, act with integrity, and who want to grow while making a real impact on patient supply. This role offers growth, visible impact across global supply, and the chance to help GSK unite science, technology and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead technical strategy, troubleshooting, manufacturing scale-up activities, process robustness initiatives, technology transfers., lifecycle changes and technical reviews. - Provide SME leadership for investigations, root cause analysis, corrective and preventive actions, and regulatory responses. - Translate lab and development knowledge into robust, scalable manufacturing processes. - Design and run experiments for process characterization, optimization and validation. - Support inspection readiness and audit activities. - Define and deploy process control strategies, performance standards, and lifecycle monitoring for manufacturing processes. - Provide technical input to change controls, risk assessments and corrective actions. - Train, coach, and mentor cross-functional teams and MSAT peers to build capability and share best practice across the network. - Drive continuous improvement by identifying technical improvements, leading implementation, and tracking outcomes. Why You? Work arrangement This role is hybrid. You will be expected to be on-site regularly to support manufacturing and operational readiness activities as well as technical transfer work. Exact on-site vs remote days will be agreed with your manager based on project needs. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Bachelor's degree in a relevant scientific or engineering discipline such as Pharmaceutical Sciences, Chemical Engineering, Biology, or Chemistry. - 5+ years' experience in pharmaceutical vaccines or biologics manufacturing technical operations. - Hands-on experience with technology transfers, scale-up, process validation, and lifecycle management in a regulated environment. - Practical knowledge of unit operations such as mixing/homogeneity, chromatography, filtration, ultrafiltration/diafiltration, and aseptic processing. - Demonstrated experience leading technical investigations, root cause analysis, and CAPA development. - Experience using data analysis and advanced statistical methods for process understanding. - Knowledge of GMP and regulatory expectations relevant to manufacturing and quality systems. Preferred Qualification If you have the following characteristics, it would be a plus - Advanced degree (Master's or PhD) in a relevant field. - Experience with sterile manufacturing and aseptic processing. - Background in extractables and leachable, material qualification, or supplier component assessments. - Knowledge of regulatory expectations for process validation and continued process verification. - Experience leading cross-functional projects and mentoring technical teams. - Formal training in project management, risk management, or continuous improvement methods (for example Lean or Six Sigma). - Proven track record of leading cross-functional teams and influencing in a matrix environment. - Experience preparing for and supporting regulatory inspections and responses. - Strong written and verbal communication skills for clear technical reporting and stakeholder engagement. What we value in you - Practical, clear communication and a collaborative mindset. - Curiosity and a willingness to learn and share knowledge. - A focus on patient safety, quality and continuous improvement.