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 SUMMARYThe Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings Structural/Civil Biotech process a

JOB SUMMARYThe Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings Structural/Civil Biotech process a

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:The Manufacturing Associate I/II is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure a

Position Summary:The Manufacturing Associate I/II is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure a

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

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 SUMMARYThis position is on a 2-2-3 rotating schedule dayshift (7am-7pm)The Manufacturing Associate I/II is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure all wor

JOB SUMMARYThis position is on a 2-2-3 rotating schedule dayshift (7am-7pm)The Manufacturing Associate I/II is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure all wor

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

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

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

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

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

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

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

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

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

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 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

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

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