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

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

The Analytical and Formulation Sciences (AFS) unit of the KBI Commercial Manufacturing Site executes various analytical activities in support of commercial manufacturing, release, and stability. The Project Leader will supervise the daily aspects within the project as well as define activities and manage meeting deliverables internally and externally. The Project Leader m

The Facilities Engineering Intern will interact with a diverse group of people in support of the Facilities Engineering Department. The Facilities Engineering Intern will participate in the technical aspects of capital project implementation to ensuring the project's success in meeting its respective objectives. Technical aspects may include Develop, evaluate, and design

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

The Operational Excellence (OpEx) Senior Specialist or Manager will support the site's portfolio of continuous improvement initiatives, activities, and high value projects. The Sr OpEx Specialist will manage several projects concurrently, coach leaders through the successful execution of improvement events, and capture significant sustained value for our customers. The Sr

The Senior Manufacturing Associate I/II is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Senior Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted "Right First Time" (RFT) following Good Manufacturing Practices (GMP), Good Document

This position is on a 2 2 3 shift, with the hours 7p 7a. The Sr. 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 Sr. Manufacturing Associate I/II Downstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally,

This position operates on a 2 2 3 schedule with the hours 7 00 am 7 30 pm. The Manufacturing Assistant position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleanings and maintains gowning supplies for the locker rooms and gowning rooms at the CMF GMP facility to support continuous manufacturing opera

We are currently seeking a highly motivated and detail oriented individual to fill the role of Inside Sales Sr. Technical Lead. This position will report to the Associate Director, Contracts, Inside Sales, and Analytics and will be responsible for prospecting, lead generation, and lead management. Through effective prospecting, they will build and expand the corporate cli

The Supply Chain Operations Analyst (Intern) is accountable for the design and execution of demand planning and order forecasting, supply planning, product deployment and expediting processes and the development and implementation of a stocking optimization model to minimize costs and inventory while delivering on service requirements. Position Responsibility Research and

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L

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