Global AS&T Lead
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Summary #LI-Hybrid Primary Location: Barcelona, Spain Relocation Support: This role is based in Barcelona, Spain. Novartis is unable to offer relocation support: please only apply if accessible. Imagine shaping how analytical laboratories operate across a global network and turning scientific excellence into meaningful transformation. As Global AS&T Lead, you will bring together analytical expertise, strategic thinking and change leadership to advance laboratory technologies, harmonize ways of working, and accelerate automation, digitalization and artificial intelligence-enabled solutions. Working across Quality, Manufacturing, Development, Regulatory, Digital and Engineering, you will influence high-impact decisions and help build scalable, future-ready laboratory capabilities that strengthen operations and ultimately support patients worldwide.
About the Role
Key Responsibilities:- Shape the global RLT laboratory transformation roadmap, translating strategic priorities into measurable, scalable initiatives.
- Guide site Quality Control and Analytical Science and Technology teams on complex scientific, technical, and compliance decisions.
- Establish cross-site governance, technical standards and portfolio priorities for analytical sciences and laboratory technologies.
- Drive harmonization of analytical methods, laboratory processes, equipment strategies and capabilities across the global network.
- Lead automation, digitalization and artificial intelligence-enabled laboratory transformation to deliver scientific and operational value.
- Represent Analytical Science and Technology in major technology transfers, laboratory expansions and global technology deployments.
- Partner across Quality, Manufacturing, Development, Regulatory, Digital and Engineering to enable integrated, network-wide solutions.
- Strengthen the global Analytical Science and Technology community through coaching, knowledge sharing and capability building.
- Degree in Chemistry, Pharmaceutical Sciences, Pharmacy, Biochemistry or a related scientific discipline.
- Significant experience in analytical sciences, quality control, analytical development or technical operations within a regulated pharmaceutical environment.
- Strong knowledge of Good Manufacturing Practice, pharmaceutical quality systems, data integrity, validation and regulatory expectations.
- Deep expertise in chromatographic techniques, analytical troubleshooting, method lifecycle management, validation, transfer and laboratory investigations.
- Strong strategic thinking and decision-making skills, with the ability to address complex scientific and network-level challenges.
- Excellent communication and influencing skills, fluent English, and willingness to travel internationally approximately 25% of the time.
- Experience with radiopharmaceuticals and Radioligand Therapy.