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

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 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

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

The Manufacturing Compliance Intern will apply scientific principles to support batch report generation, manufacturing record review, and manufacturing improvement projects including CAPAs and manufacturing document revisions. This role will provide exposure to biopharmaceutical manufacturing operations in a cGMP manufacturing facility which also includes pre quality revi

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

Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new scientific and strategic partnerships, collaborations, licensing opportunities, joint ventures and alliances. Establishes and implements appropriate development strategies to suppo

Seeking a highly motivated and detail oriented intern to assist with data cleanup in our Salesforce instance. This internship opportunity will provide valuable experience in data management and contribute significantly to the enhancement of our overall operational efficiency. Term May 20th August 9th, 2024. Responsibilities The intern will be responsible for Identifying a

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

This position is on a 4 3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Position Responsibilities Execution of procedures for microbial manufacturing without minimal supervision

This position will be on a 4 3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high quality levels Position Responsibilities Assist in the execution of procedures for microbial manufactur

This position will be on a 4 3 night shift schedule. The hours are 7 00 pm to 7 00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high quality levels Position Responsibilities Assist in the execution of procedures for microbial ma