Teams at Lonza

Pharmaceutical manufacturing intern supporting fill-and-finish operations across manufacturing, quality, development, and MSAT teams. Responsibilities include learning pharmaceutical processes, following cGMP and safety requirements, developing procedures, troubleshooting process issues, organizing documentation, and supporting day-to-day site operations under supervision.

Supports downstream purification development for recombinant protein therapeutics. Performs chromatography, filtration, viral clearance, sampling, testing, and data collection; prepares buffers and reagents; operates purification equipment; assists with technology transfer, process optimization, and characterization studies; troubleshoots experimental issues; and maintains EHS, quality, cGMP, and data integrity compliance in a site-based laboratory.

Manufactures therapeutic proteins under cGMP conditions in cleanroom environments. Performs equipment monitoring, laboratory sampling, sanitization, aseptic handling, equipment preparation and operation, CIP/SIP activities, troubleshooting, materials and solutions preparation, and process documentation. Uses SOPs, logbooks, batch records, and LIMS while developing competency in biopharmaceutical manufacturing operations through a 15-month structured training program.