KBI Biopharma

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

Job SummaryResponsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring of protocols test scripts and data tables to fac

Job SummaryResponsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring of protocols test scripts and data tables to fac

Job SummaryThe Laboratory Information Management System (LIMS) Administrator serves as the primary system administrator and technical expert for the laboratorys LIMS platform. This position is responsible for supporting system users configuring and maintaining laboratory workflows man

Job SummaryThe Laboratory Information Management System (LIMS) Administrator serves as the primary system administrator and technical expert for the laboratorys LIMS platform. This position is responsible for supporting system users configuring and maintaining laboratory workflows man

Position Summary: The QA Manager/Sr. Manager manages a team of QA Specialists and the process for the QA oversight of Deviations and CAPAs. This team performs daily deviation triage (classification) and investigation review/approval. The team is also responsible for QA oversight of th

Position Summary: The QA Manager/Sr. Manager manages a team of QA Specialists and the process for the QA oversight of Deviations and CAPAs. This team performs daily deviation triage (classification) and investigation review/approval. The team is also responsible for QA oversight of th

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

Job summaryThe Director Operational Excellence is responsible for leading the Boulder sites Operational Excellence strategy and a global portfolio of continuous improvement initiatives transformational projects and Lean maturity programs that drive sustainable business performance and

Job summaryThe Director Operational Excellence is responsible for leading the Boulder sites Operational Excellence strategy and a global portfolio of continuous improvement initiatives transformational projects and Lean maturity programs that drive sustainable business performance and

The EHS&S Specialist assists the sites Environment Health Safety andSustainable Development Head for the implementation of the EnvironmentalHealth Safety and Sustainability (EHSS) program.Main part of the mission is to manage the environmental and sustainability part of site program a

The EHS&S Specialist assists the sites Environment Health Safety andSustainable Development Head for the implementation of the EnvironmentalHealth Safety and Sustainability (EHSS) program.Main part of the mission is to manage the environmental and sustainability part of site program a

Position Summary:The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing.This position performs all routine/non-routine cleaning of equipment prepares buffers/medias glass wash of misc. parts assembles setups and filters autoclaves me

Position Summary:The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing.This position performs all routine/non-routine cleaning of equipment prepares buffers/medias glass wash of misc. parts assembles setups and filters autoclaves me

This position is on 2-2-3 shifts 7a-7p and 7p-7a. MFG Support Associate I/II is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Manufacturing Associate I/II Support must follow the instructions depicted in SRs (Medi

This position is on 2-2-3 shifts 7a-7p and 7p-7a. MFG Support Associate I/II is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Manufacturing Associate I/II Support must follow the instructions depicted in SRs (Medi

*Nightshift: 6PM-6AM 2-2-3 rotating scheduleThe Senior Manufacturing Associate I/II (Days) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow writ

*Nightshift: 6PM-6AM 2-2-3 rotating scheduleThe Senior Manufacturing Associate I/II (Days) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow writ

*Nightshift: 6PM-6AM 2-2-3 rotating scheduleThe Senior Manufacturing Associate I/II (Nights) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow wr

*Nightshift: 6PM-6AM 2-2-3 rotating scheduleThe Senior Manufacturing Associate I/II (Nights) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow wr

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

JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respe

JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respe

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