Teams at Lonza

Manages customer-facing scientific programs for bioscience products, translating client needs into execution plans and coordinating cross-functional delivery. Oversees contractual obligations, client relationships, risks, escalations, media development, non-GMP pilot activities, product supply, forecasting, client visits, and business reviews. Supports regional testing clients and new system installations while maintaining demand signals through SAP IBP. Requires life sciences or equivalent experience, FDA-regulated biotech or pharma experience, CDMO knowledge, strong communication skills, and project or client management expertise.

Provide QA oversight for GMP biopharmaceutical manufacturing: review and approve SOPs, batch records, lead investigations (deviations, CAPA, change control), support audits/inspections, manage small projects, and train/audit internally to ensure regulatory compliance and batch disposition.

Performs material and equipment preparation for cGMP biopharmaceutical manufacturing. Maintains cleanrooms, sanitizes equipment, conducts basic laboratory measurements, executes SOPs and batch records, submits samples through LIMS, and supports quality, validation, environmental monitoring, deviations, and data integrity activities. Collaborates with Manufacturing, MSAT, and QA teams while working rotating 12-hour shifts in a cleanroom environment.