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

This Manufacturing Sciences and Technology (MS&T) Principal Engineer position will lead a team responsible for process development, and process transfer for clinical and commercial manufacturing. This person and their team will also have responsibilities for the ownership of processing equipment and unit operations, including system design, procurement, installation, and

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 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 supervisi

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

This position will be on a 2 2 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 manufact

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

This position is on a 2 2 3 night shift schedule. The hours are 7 00 pm to 7 00 am. 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 s

Effectively leads a team within Program Management or large Project Management function, ensures appropriate development and control of related processes and systems. With personal responsibility for a portfolio, the role holder is the primary client account and relationship manager for KBI PMO, driving business delivery and exemplary client service to maximum benefit for

This position represents an opportunity to apply engineering expertise at the Engineer II level in the Manufacturing Sciences and Technology group in support of GMP production operations at the Boulder, Colorado manufacturing facility. Position Responsibilities Qualified candidates would have the ability to provide biological engineering principles to the process developm

Responsible for independent problem solving. Specialized in at least one discipline that is directly applicable to the job function. Execute components of a project. Focus on meeting deliverables. Position Responsibilities Develops, leads and supports a team responsible for downstream process development and manufacturing activities. Conceptualizes, proposes and executes

This position will be on a 2 2 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

Responsible for independent problem solving. Specialized in at least one discipline that is directly applicable to the job function. Execute components of a project. Focus on meeting deliverables. Position Responsibilities Develops, leads and supports a team responsible for upstream process development and manufacturing activities. Conceptualizes, proposes and executes th

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 responsible for providing engineering support and owns multiple systems, processes, or areas. This position will primarily provide technical support of clean utilities and HVAC operations supporting a biologics production facility. This work includes working independently and with Manufacturing Operations, Quality, Outside Contractors, site IT and Manufac