KBI Biopharma

This is a hybrid position based in Durham NC.POSITION SUMMARYThe SAP Systems Analyst supports the implementation enhancement and ongoing support of SAP S/4HANA supply chain business processes within a regulated pharmaceutical environment. This role focuses on delivering functional sol

This is a hybrid position based in Durham NC.POSITION SUMMARYThe SAP Systems Analyst supports the implementation enhancement and ongoing support of SAP S/4HANA supply chain business processes within a regulated pharmaceutical environment. This role focuses on delivering functional sol

Job Description 7AM-7PM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I/II 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 records and GMP

Job Description 7AM-7PM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I/II 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 records and GMP

Job Summary:The Senior Quality Systems Architect is a highly experienced individual contributor responsible for the design development implementation and ongoing support of GxP-regulated Quality applications within a biopharmaceutical environment.The role operates with a high degree o

Job Summary:The Senior Quality Systems Architect is a highly experienced individual contributor responsible for the design development implementation and ongoing support of GxP-regulated Quality applications within a biopharmaceutical environment.The role operates with a high degree o

Position Summary:Responsible for supporting microbiological programs and testing activities for processes instruments and equipment. ensures the effective use of material equipment and personnel while developing products and processes at high quality levels.This person is responsible

Position Summary:Responsible for supporting microbiological programs and testing activities for processes instruments and equipment. ensures the effective use of material equipment and personnel while developing products and processes at high quality levels.This person is responsible

Position SummaryResponsible for supporting process development activities for downstream production processes instruments and equipment.Position ResponsibilitiesSupport all downstream process development activities including execution of experiments compilation and analysis of data an

Position SummaryResponsible for supporting process development activities for downstream production processes instruments and equipment.Position ResponsibilitiesSupport all downstream process development activities including execution of experiments compilation and analysis of data an

JOB SUMMARYThe Director has overall responsibility for the companys Environmental Health Safety and Sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufact

JOB SUMMARYThe Director has overall responsibility for the companys Environmental Health Safety and Sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufact

JOB SUMMARYThe Director has overall responsibility for the companys Environmental Health Safety and Sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufact

JOB SUMMARYThe Director has overall responsibility for the companys Environmental Health Safety and Sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufact

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