Position Summary:KBI Biopharma seeks to fill a role for Upstream Cell Culture Process Development Associate. This person will lead and assist in cell culture and harvest projects for mammalian cell lines (mainly CHO variants) in support of process development scale-up and technology t

Position Summary:KBI Biopharma seeks to fill a role for Upstream Cell Culture Process Development Associate. This person will lead and assist in cell culture and harvest projects for mammalian cell lines (mainly CHO variants) in support of process development scale-up and technology t

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Full Time

Position Summary: The Downstream Process Development Associate II supports and executes laboratory studies within the KBI Biopharma (KBI) Downstream Process Development organization under general supervision.Position Responsibilities: Conducts laboratory experiments in support of down

Position Summary: The Downstream Process Development Associate II supports and executes laboratory studies within the KBI Biopharma (KBI) Downstream Process Development organization under general supervision.Position Responsibilities: Conducts laboratory experiments in support of down

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Full Time

JOB SUMMARY*Dayshift 7am-7pm 2-2-3 rotating scheduleThe Manufacturing Support Associate I/II position is designed as an introduction to the environment of cGMP manufacturing. This position performs all routine/nonroutine cleanings of the GMP Facilities manages Process Waste and contin

JOB SUMMARY*Dayshift 7am-7pm 2-2-3 rotating scheduleThe Manufacturing Support Associate I/II position is designed as an introduction to the environment of cGMP manufacturing. This position performs all routine/nonroutine cleanings of the GMP Facilities manages Process Waste and contin

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JOB SUMMARY *Dayshift: 6AM-6PM 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 f

JOB SUMMARY *Dayshift: 6AM-6PM 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 f

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Full Time

Job Summary*Nightshift 7PM-7AM 2-2-3 rotating scheduleThe Manufacturing Associate II (Nights) is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II must

Job Summary*Nightshift 7PM-7AM 2-2-3 rotating scheduleThe Manufacturing Associate II (Nights) is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II must

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Full Time

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

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

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JOB SUMMARY *Nightshift: 7PM-7AM 2-2-3 rotating 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 SUMMARY *Nightshift: 7PM-7AM 2-2-3 rotating 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

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Full Time

Job DescriptionThe calibration technician works within a team environment that actively supports participates and embraces an empowered team culture including significant interaction with Quality Assurance Manufacturing Operations Engineering and other support groups.Perform Calibrati

Job DescriptionThe calibration technician works within a team environment that actively supports participates and embraces an empowered team culture including significant interaction with Quality Assurance Manufacturing Operations Engineering and other support groups.Perform Calibrati

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Kbi Biopharma

Full Time

JOB SUMMARYThe Manufacturing Science and Technology (MS&T) Director or Senior Director is responsible for establishing and directing the execution resources business processes and best practices for tech transfer process validation and support laboratory activities for the MS&T depart

JOB SUMMARYThe Manufacturing Science and Technology (MS&T) Director or Senior Director is responsible for establishing and directing the execution resources business processes and best practices for tech transfer process validation and support laboratory activities for the MS&T depart

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Full Time

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

Apply Now
Full Time

JOB SUMMARY The Global Supply Chain Material Planning Manager will report to the Sr Manager of Global Supply Chain Planning. The Global Supply Chain Material Planning Manager will be client facing by participating Joint Steering Committees. (S)he will directly manage the end to end ba

JOB SUMMARY The Global Supply Chain Material Planning Manager will report to the Sr Manager of Global Supply Chain Planning. The Global Supply Chain Material Planning Manager will be client facing by participating Joint Steering Committees. (S)he will directly manage the end to end ba

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Full Time

JOB 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 procedures and for

JOB 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 procedures and for

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Full Time

JOB 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 procedures and for

JOB 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 procedures and for

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Full Time

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/

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Full Time

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

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Full Time

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

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Full Time

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

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Full Time

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

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Full Time

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

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Kbi Biopharma

Full Time

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

Apply Now