KBI Biopharma

Job Summary:Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification initiation in EtQ and closure. Support external client review and resolution of comments for assigned deviations and C

Job Summary:Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification initiation in EtQ and closure. Support external client review and resolution of comments for assigned deviations and C

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

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: Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Formulation and Stability (AFS) Department. This role is responsible for executing experimental pro

Position Summary: Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Formulation and Stability (AFS) Department. This role is responsible for executing experimental pro

Position SummaryThe Lab and Manufacturing Systems Support Analyst will provide IT support for KBI Biopharmas laboratory and manufacturing environments and be the primary contact for issues related to Lab and Manufacturing Systems as they relate to IT. The position will require basic I

Position SummaryThe Lab and Manufacturing Systems Support Analyst will provide IT support for KBI Biopharmas laboratory and manufacturing environments and be the primary contact for issues related to Lab and Manufacturing Systems as they relate to IT. The position will require basic I

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: 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 Description 7PM-7AM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I/II - Solution Prep 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

Job Description 7PM-7AM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I/II - Solution Prep 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

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:Perform data review for commercial program documents including Process Performance Verification (PPQ) reports Continuous Process Verification (CPV report) and any other reports supporting process validation for monoclonal antibodies recombinant proteins peptides and other

Job Summary:Perform data review for commercial program documents including Process Performance Verification (PPQ) reports Continuous Process Verification (CPV report) and any other reports supporting process validation for monoclonal antibodies recombinant proteins peptides and other

Job DescriptionThis individual will provide thought-leadership expertise and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. Individual will be responsible for the valid

Job DescriptionThis individual will provide thought-leadership expertise and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. Individual will be responsible for the valid

TRAVEL: 10% domestic travel requiredHOURS: Full Time/40 hoursJOB DUTIES: Design implement and manage local and wide-area networks (LAN/WAN). Configure and maintain network devices such as switches routers and firewalls. Troubleshoot network connectivity issues and resolve basic networ

TRAVEL: 10% domestic travel requiredHOURS: Full Time/40 hoursJOB DUTIES: Design implement and manage local and wide-area networks (LAN/WAN). Configure and maintain network devices such as switches routers and firewalls. Troubleshoot network connectivity issues and resolve basic networ

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

Please Note: This is a day shift opportunity that follows a 2-2-3 schedule.Job SummaryThe QA Manufacturing Specialist is responsible for ensuring raw materials products processes facilities documentation and systems conform to quality standards internal procedures systems and governme

Please Note: This is a day shift opportunity that follows a 2-2-3 schedule.Job SummaryThe QA Manufacturing Specialist is responsible for ensuring raw materials products processes facilities documentation and systems conform to quality standards internal procedures systems and governme