KBI Biopharma

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

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

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: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

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