Teams at Lonza

Leads global corporate cGMP audits across pharmaceutical and medical device operations. Advises manufacturing sites on regulatory compliance, remediation, inspection readiness, supplier quality, and risk mitigation. Acts as a supplier portfolio SPOC, performs quality assessments, monitors compliance risks, and mentors auditors. Requires prior MHRA or HPRA health authority inspection experience, extensive cGMP auditing expertise, and an advanced scientific degree.

Manage gLIMS master data, validation testing, system reviews, KPI reporting, compliance documentation, and data quality activities. The role supports LabVantage LIMS operations across global and local teams, investigates system issues, contributes to continuous improvement, and provides end-user support in a regulated pharmaceutical environment.

Designs, configures, tests, commissions, validates, and maintains integrated automation and control systems. Supports PLC, SCADA, drive, servo, and vision systems; creates functional and design specifications; maintains technical documentation and software backups; troubleshoots control wiring; coordinates projects and continuous improvement; and provides rotating after-hours plant support.