The Manufacturing Biotechnologist Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I Biotechnologists are expected to execute process recipes, follow written procedures (SOPs), monitor eq...
The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and ...
Key Responsibilities: Document writing for transfers/validations/investigations Perform assay work for transfers/validations/investigations Leads set up and verification of electronic equipment/templates/forms for transfers/validat...
The Director, Commercial Development will be responsible for developing and commercializing targeted business, & offerings approaches and operative pricing strategies that facilitate the Mammalian BU’s expansion strategy. The Director ensur...
Manufacturing Suite Point of Contact Role Purpose The role of the Manufacturing Suite Point of Contact is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. This positi...
The Manufacturing Associate Level II is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level II associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment an...
The Asset Business Partner is an integral member of the Asset Leadership team and a regular participant in asset and functional strategy setting. The BP is responsible for creating and maintaining a comprehensive resource plan and schedule ...
Customer Service Procedures, SOP and SDS requirements. Lonza's certification requires compliance with these procedures..., verbal updates and release notifications. Help customers with Lonza.com website registration, order placement, including...