KBI Biopharma

Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring of protocols test scripts and data tables to facilitate col

Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring of protocols test scripts and data tables to facilitate col

JOB SUMMARYThe Downstream Process Development (PD) Associate Scientist provides process development input and co-ownership for a product including all development and design decisions with oversight and mentorship from senior process development staff. They learn to apply scientific p

JOB SUMMARYThe Downstream Process Development (PD) Associate Scientist provides process development input and co-ownership for a product including all development and design decisions with oversight and mentorship from senior process development staff. They learn to apply scientific p

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

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

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

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

JOB SUMMARY: The 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

JOB SUMMARY: The 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

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

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

JOB SUMMARY The manufacturing support Manager/Sr Manager will oversee the manufacturing support activities including solution prep finite scheduling for solution prep material control and GMP cleaning. The individual will lead the manufacturing support team with the aim of achieving s

JOB SUMMARY The manufacturing support Manager/Sr Manager will oversee the manufacturing support activities including solution prep finite scheduling for solution prep material control and GMP cleaning. The individual will lead the manufacturing support team with the aim of achieving s

JOB SUMMARYThe Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respec

JOB SUMMARYThe Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respec

Position Summary:General responsibility for the installation 24/7 day-to-day operation maintenance and modification of all KBI Biopharma site systems. This position is also responsible for repairs troubleshooting corrective (repair/unplanned/modification) and preventative (planned) ma

Position Summary:General responsibility for the installation 24/7 day-to-day operation maintenance and modification of all KBI Biopharma site systems. This position is also responsible for repairs troubleshooting corrective (repair/unplanned/modification) and preventative (planned) ma

About this job:Join KBI Biopharmas Corporate Accounting team as a Senior Accountant and play a pivotal role in driving financial excellence for a leading global CDMO advancing life-saving therapies. This high-impact position combines technical accounting expertise with strategic busin

About this job:Join KBI Biopharmas Corporate Accounting team as a Senior Accountant and play a pivotal role in driving financial excellence for a leading global CDMO advancing life-saving therapies. This high-impact position combines technical accounting expertise with strategic busin

Please Note: This position is Wednesday-Saturday 2nd Shift Swing (4pm - 2am)Job Summary: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 f

Please Note: This position is Wednesday-Saturday 2nd Shift Swing (4pm - 2am)Job Summary: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 f

Position SummaryThis position operates on a night shift 2-2-3 schedule. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manu

Position SummaryThis position operates on a night shift 2-2-3 schedule. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manu

The Project Manager CAPEX is responsible for leading projects from requirements definition through deployment identifying schedules scopes budget estimations and implementation plans including risk mitigation. They will perform the following objectives:Coordinate internal and external

The Project Manager CAPEX is responsible for leading projects from requirements definition through deployment identifying schedules scopes budget estimations and implementation plans including risk mitigation. They will perform the following objectives:Coordinate internal and external

JOB SUMMARYThe Manufacturing Execution System (MES) engineer on the MES operations team will support the startup and ongoing manufacturing operations at a biopharmaceutical manufacturing facility. The individual will report to the Associate Director of MES Operations. The individual

JOB SUMMARYThe Manufacturing Execution System (MES) engineer on the MES operations team will support the startup and ongoing manufacturing operations at a biopharmaceutical manufacturing facility. The individual will report to the Associate Director of MES Operations. The individual

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 PD Scientist II provides process development ownership for a product including all development and design decisions with some oversight and supervision. They can apply advanced scientific principles to design and execute laboratory studies for unit operation devel

Position Summary:The PD Scientist II provides process development ownership for a product including all development and design decisions with some oversight and supervision. They can apply advanced scientific principles to design and execute laboratory studies for unit operation devel