The incumbent will have Operation Excellence / Lean Six Sigma expertise and ideally manufacturing, process development and/or new technology introduction experience. The incumbent will support and manage key Manufacturing continuous improvement initiatives and high value cross functional projects. Incumbent will actively manage several projects concurrently. Job Responsib

Responsible for contributing to the development, maintenance, and continuous improvement of the GMP Training Program. Facilitate projects and training initiatives that drive quality, compliance, and operational effectiveness for the organization. Develop training materials and provide guidance in development and implementation of a consistent training program. Assess new

Responsible for reception area and acts as receptionist for visitors. Assist site leadership in the facility and administrative management of the Leuven, Belgium site. Job responsibilities Maintain office services by organizing office operations and procedures. Place and manage supply requisitions. Coordinate orientation and training of employees. Coordinate receipt and s

This position is on a 2 2 3 shift, 7a 7p. The Manufacturing Associate I/II Downstream is responsible for the execution of production activities for early and late phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II Downstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally, must ensure all work i

The Manufacturing Sciences & Technology (MS&T) Technology Transfer (TT) Intern will apply sound scientific and engineering principles to support the transfer and enrollment of new biopharmaceutical processes and/or to support the ongoing production activities in the cGMP manufacturing facility. The scope of this role includes Supporting technology transfer for manufacturi

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. This person is responsible for the

This position is on 2 2 3 shifts, 7p 7a. The Sr. Manufacturing Associate I/II MFG Support is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Sr. Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure

The Manufacturing Sciences & Technology (MS&T) Technology Transfer (TT) Intern will apply sound scientific and engineering principles to support the transfer and enrollment of new biopharmaceutical processes and/or to support the ongoing production activities in the cGMP manufacturing facility. The scope of this role includes Supporting technology transfer for manufacturi

This position is on 2 2 3 shifts, 7a 7p. The Sr. Manufacturing Associate I/II MFG Support is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Sr. Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure

To provide Metrology support and services to KBI's internal operations. Shift Schedule Monday Friday 8 30 am 5 30 pm Position Responsibilities Perform scheduled calibrations on equipment and systems in the facility, which include Manufacturing, Analytical Labs, Utilities, and Warehouse. Manage and maintain instrument calibration documentation and CMMS database. Responsibl

The Manufacturing Sciences & Technology (MS&T) Technology Transfer (TT) Intern will apply sound scientific and engineering principles to support the transfer and enrollment of new biopharmaceutical processes and/or to support the ongoing production activities in the cGMP manufacturing facility. The scope of this role includes Supporting technology transfer for manufacturi

The manufacturing execution system engineer on the technical support and investigations team will support the startup and ongoing manufacturing operations at a new biopharmaceutical manufacturing facility. During startup the individual will be responsible for supporting the introduction and qualification of the MES system at the facility. The individual will report to the

This position operates on a 2 2 3 schedule, with 7 00 pm 7 00 am shifts. The Manufacturing Supervisor leads a team of manufacturing associates to perform upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Supervisor will plan, assign, and monitor daily tasks to ensure timely "Right First Time" execution

Perform the day to day management and distribution of a rapidly growing library of biologics samples. Will be responsible for checking in, registering, and aliquoting new samples, maintaining database and Access/Excel inventories, and labeling and distributing outgoing samples. Will work closely with basic automation (i.e. Tube Cappers, barcode readers, automated liquid h

This position will provide validation support for at least one of the following areas Facilities qualification Utilities qualification Equipment qualification Manufacturing process control system qualification Cleaning validation Computer system validation The incumbent will support data retrieval, compilation, verification, and comparative analysis from a variety of pape