KBI Biopharma

Job Description Day Shift / 7PM -7AM / 2-2-3 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 Day Shift / 7PM -7AM / 2-2-3 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 SummaryThe Facilities Engineering Department is responsible for maintaining the site infrastructure in a safe compliant and reliable state to support cGMP manufacturing operations. The department oversees the maintenance and reliability of building systems structural and architect

Job SummaryThe Facilities Engineering Department is responsible for maintaining the site infrastructure in a safe compliant and reliable state to support cGMP manufacturing operations. The department oversees the maintenance and reliability of building systems structural and architect

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support program te

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support program te

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

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

JOB DESCRIPTIONSolution Prep Manufacturing Supervisor 12 hour Night Shift 2*2*3 Schedule The Manufacturing Supervisor Solution Prep leads a team of manufacturing associates to perform both upstream and downstream preparation of solutions and growth media used for processing of bulk in

JOB DESCRIPTIONSolution Prep Manufacturing Supervisor 12 hour Night Shift 2*2*3 Schedule The Manufacturing Supervisor Solution Prep leads a team of manufacturing associates to perform both upstream and downstream preparation of solutions and growth media used for processing of bulk in

Job DescriptionPosition 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

Job DescriptionPosition 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

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

KBI Biopharma is seeking a highly skilled and motivated Analytical Scientist to join our Analytical and Formulation Sciences (AFS) team in Durham NC. This role is ideal for a PhD-level scientist with deep expertise in protein analytics ideally with a background in formulation developm

KBI Biopharma is seeking a highly skilled and motivated Analytical Scientist to join our Analytical and Formulation Sciences (AFS) team in Durham NC. This role is ideal for a PhD-level scientist with deep expertise in protein analytics ideally with a background in formulation developm

At KBI we are creating planning processes to support the companys growth and position it as the next generation CDMO. The Global Supply Chain Sr. Planning is a unique role to lead global Material Planning and Execution with the two ultimate goals of ensure that accurate and compliant

At KBI we are creating planning processes to support the companys growth and position it as the next generation CDMO. The Global Supply Chain Sr. Planning is a unique role to lead global Material Planning and Execution with the two ultimate goals of ensure that accurate and compliant

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 SUMMARYThe SAP Enterprise Data Architect role provides expertise in SAP S/4HANA data architecture enterprise data modeling migration strategy and data governance. This is a key role in designing scalable data structures across source staging and target environments; defining migra

JOB SUMMARYThe SAP Enterprise Data Architect role provides expertise in SAP S/4HANA data architecture enterprise data modeling migration strategy and data governance. This is a key role in designing scalable data structures across source staging and target environments; defining migra

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

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

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

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

Job Description 7AM-7PM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I 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/GD

Job Description 7AM-7PM / 2*2*3 Manufacturing ScheduleThe Manufacturing Associate I 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/GD

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 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