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

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

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

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 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

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 Senior Inventory Accountant role is primarily responsible for ensuring the accurate and complete accounting for and reporting of the company's inventory. The position is a part of corporate accounting team and will partner with Supply Chain, IT and other teams throughout the organization. Responsibility Responsible for performing monthly inventory related general ledg

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 Maintenance and Facilities Manager is responsible for ensuring buildings, equipment and systems are maintained and fit for use. The Manager oversees day to day maintenance and calibration operations including planning and scheduling, coordination of work order execution, troubleshooting and problem solving, and ensuring quality and completeness of all associated docum

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

Reviews data associated with development and qualification of analytical methods and testing of in process and drug substance/product samples. Position Responsibilities Reviews data and reports associated with development and qualification of analytical methods and testing of in process and drug substance/drug product samples. Verifies that calculations and documented inf

Manages all activities related to the planning, purchase, receipt, warehousing, and distribution of supplies and materials used in the company's development, production, and administrative support functions. Position Responsibilities Execute the daily operations of inventory planning and procurement areas in the development and execution of short and long range production

General responsibility for the installation, day to day 24/7 operation, maintenance, and modification of all KBI Biopharma site systems. This position is also responsible for repairs, troubleshooting, corrective (repair/unplanned/modification) and preventative (planned) maintenance of associated systems and equipment. The technician must be able to work both independently