RA RIB Surveillance Specialist

Conduct worldwide regulatory intelligence surveillance across major global health authorities (FDA, EMA, MHRA, PMDA, Health Canada, ICH, PIC/S) for human and veterinary medicines.

Synthesize complex regulatory updates, guidance documents, and Q&A texts into actionable summary reports and pre-assess potential impact on Lonza's CDMO offerings.

Partner with global Regulatory Subject Matter Experts (SMEs), Quality, and cross-functional teams to lead intelligence assessment meetings and track resulting action items.

Maintain regulatory intelligence databases, Power BI/Tableau metrics dashboards, and indexed guidance libraries to ensure global visibility and audit readiness.

Build internal training materials to enhance regulatory intelligence capabilities and proactively identify regulatory risks and opportunities across the network.