KBI Biopharma

The Manufacturing Science and Technology (MS&T) Senior Engineer is responsible for technology transfer activities (mainly downstream focused) document authoring/review and manufacturing facility support to ensure client program success. The role requires significant collaboration with

The Manufacturing Science and Technology (MS&T) Senior Engineer is responsible for technology transfer activities (mainly downstream focused) document authoring/review and manufacturing facility support to ensure client program success. The role requires significant collaboration with

Job SummaryIndividual contributor and special project leader responsible for ensuring compliance with internal quality documents regulatory requirements and cGMP. The incumbent will serve as Quality-to-Quality client liaison and sometimes SME for the Quality team reporting cross-QA me

Job SummaryIndividual contributor and special project leader responsible for ensuring compliance with internal quality documents regulatory requirements and cGMP. The incumbent will serve as Quality-to-Quality client liaison and sometimes SME for the Quality team reporting cross-QA me

Position Summary:The Program Integration Associate II independently coordinates planning integration and execution-readiness activities across process development and CMC programs. The position applies technical and operational knowledge to support facility fit assessments BOM forecas

Position Summary:The Program Integration Associate II independently coordinates planning integration and execution-readiness activities across process development and CMC programs. The position applies technical and operational knowledge to support facility fit assessments BOM forecas

JOB SUMMARYScope will include supporting all aspects of the Computer Systems Validation (CSV) Lifecycle. Employee will complete the execution and documentation of the CSV Program at the Durham facility. Employee will execute on implementation tasks work prioritization and support esca

JOB SUMMARYScope will include supporting all aspects of the Computer Systems Validation (CSV) Lifecycle. Employee will complete the execution and documentation of the CSV Program at the Durham facility. Employee will execute on implementation tasks work prioritization and support esca

The Specialist Quality Assurance Raw Materials (QARM) is responsible for quality assurance activities associated with the sampling review qualification and disposition of raw materials and consumables supporting both clinical and commercial biopharmaceutical manufacturing operations.

The Specialist Quality Assurance Raw Materials (QARM) is responsible for quality assurance activities associated with the sampling review qualification and disposition of raw materials and consumables supporting both clinical and commercial biopharmaceutical manufacturing operations.

This position is on a 2-2-3 shiftDay Shift (6am-6pm)The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate

This position is on a 2-2-3 shiftDay Shift (6am-6pm)The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate

JOB SUMMARYGeneral 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) maintena

JOB SUMMARYGeneral 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) maintena

Job Description *Night Shift / 7PM -7AM / 2-2-3 scheduleThe Manufacturing Associate I/II (Nights) will perform Upstream or Downstream production activities for early and late-phase Cell Culture programs in a GMP environment. Responsibilities include executing tasks per SOPs batch reco

Job Description *Night Shift / 7PM -7AM / 2-2-3 scheduleThe Manufacturing Associate I/II (Nights) will perform Upstream or Downstream production activities for early and late-phase Cell Culture programs in a GMP environment. Responsibilities include executing tasks per SOPs batch reco

Job DescriptionJOB DESCRIPTION:This position is on a 2-2-3 shift Day Shift (7am-7pm)The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved pro

Job DescriptionJOB DESCRIPTION:This position is on a 2-2-3 shift Day Shift (7am-7pm)The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved pro

JOB SUMMARYResponsible for overseeing microbiological programs and methods activities forprocesses instruments and equipment. Ensures the effective use of materialequipment and personnel while developing products and processes at high qualitylevels.This person is responsible for the a

JOB SUMMARYResponsible for overseeing microbiological programs and methods activities forprocesses instruments and equipment. Ensures the effective use of materialequipment and personnel while developing products and processes at high qualitylevels.This person is responsible for the a

Job SummaryThe Senior Director Warehouse Operations is responsible for strategic leadership operational performance and continuous improvement of all warehouses inventory logistics warehouse purchases warehouse systems GMP shipping and storeroom activities across KBIs North Carolina n

Job SummaryThe Senior Director Warehouse Operations is responsible for strategic leadership operational performance and continuous improvement of all warehouses inventory logistics warehouse purchases warehouse systems GMP shipping and storeroom activities across KBIs North Carolina n

Job SummaryThe Senior Director Warehouse Operations is responsible for strategic leadership operational performance and continuous improvement of all warehouses inventory logistics warehouse purchases warehouse systems GMP shipping and storeroom activities across KBIs US network. This

Job SummaryThe Senior Director Warehouse Operations is responsible for strategic leadership operational performance and continuous improvement of all warehouses inventory logistics warehouse purchases warehouse systems GMP shipping and storeroom activities across KBIs US network. This

Job summaryA Senior Software Engineer with exceptional data and software engineering skills and a passion for building data-centric applications is to join our team of software developers data scientists and product owners to support and expand KBIs Digital Transformation vision. He o

Job summaryA Senior Software Engineer with exceptional data and software engineering skills and a passion for building data-centric applications is to join our team of software developers data scientists and product owners to support and expand KBIs Digital Transformation vision. He o

At KBI Biopharma we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI where innovation mee

At KBI Biopharma we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI where innovation mee

Position Summary:The Manufacturing Associate I/II is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure a

Position Summary:The Manufacturing Associate I/II is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure a

JOB SUMMARYThe 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 a

JOB SUMMARYThe 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 a

At KBI Biopharma we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI where innovation mee

At KBI Biopharma we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI where innovation mee

Position Summary:We are seeking motivated and detail-oriented scientists to join our analytical team supporting biopharmaceutical development this role you will contribute to client-focused analytical projects by executing laboratory experiments analyzing data and collaborating with

Position Summary:We are seeking motivated and detail-oriented scientists to join our analytical team supporting biopharmaceutical development this role you will contribute to client-focused analytical projects by executing laboratory experiments analyzing data and collaborating with

Position Summary: This position resides in the Process Operations team in the Process Development department and drives robustness and consistency in the laboratory through execution and innovation of laboratory practices. They drive efficiencies in Process Development while maintaini

Position Summary: This position resides in the Process Operations team in the Process Development department and drives robustness and consistency in the laboratory through execution and innovation of laboratory practices. They drive efficiencies in Process Development while maintaini

JOB SUMMARYThis position is on a 2-2-3 rotating schedule dayshift (7am-7pm)The Manufacturing Associate I/II is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure all wor

JOB SUMMARYThis position is on a 2-2-3 rotating schedule dayshift (7am-7pm)The Manufacturing Associate I/II is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure all wor