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

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 night shift opportunity that follows a 2-2-3 scheduleJob SummaryThe QA Manufacturing Specialist II (Nights) is responsible for ensuring raw materials products processes facilities documentation and systems conform to quality standards internal procedures systems

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

JOB SUMMARY This position is responsible for the compliance review of Biopharmaceutical Development GMP data. This includes the review and approval of release in-process and stability test data. This position is also responsible for the review and approval of method qualifications and

JOB SUMMARY This position is responsible for the compliance review of Biopharmaceutical Development GMP data. This includes the review and approval of release in-process and stability test data. This position is also responsible for the review and approval of method qualifications and

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

Position SummaryThe Analytical Development (AD) unit executes analytical activities supporting the development of biologic drug substances and drug products from early development through late-phase support manufacturing. The team provides analytical leadership for non-GMP and early-p

Position SummaryThe Analytical Development (AD) unit executes analytical activities supporting the development of biologic drug substances and drug products from early development through late-phase support manufacturing. The team provides analytical leadership for non-GMP and early-p

JOB SUMMARYThe Downstream Process Development (PD) Scientist II provides process development ownership for a product including all development and design decisions with some oversight and supervision from senior process development staff. They can apply advanced scientific principles

JOB SUMMARYThe Downstream Process Development (PD) Scientist II provides process development ownership for a product including all development and design decisions with some oversight and supervision from senior process development staff. They can apply advanced scientific principles

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 DescriptionPosition Summary: The Analytical and Formulation Sciences (AFS) unit executes various analytical activities in support of internally and externally manufactured products for both non-GMP and GMP products. Activities include but not limited to: method development method

Job DescriptionPosition Summary: The Analytical and Formulation Sciences (AFS) unit executes various analytical activities in support of internally and externally manufactured products for both non-GMP and GMP products. Activities include but not limited to: method development method

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

JOB SUMMARY The Manager/Sr. Manager (Purification) manages the day-to-day affairs of an organization by assisting the Director Manufacturing in medium- and long-term scheduling strategic lead on high profile projects and to assess and respond to urgent operational issues.The individua

JOB SUMMARY The Manager/Sr. Manager (Purification) manages the day-to-day affairs of an organization by assisting the Director Manufacturing in medium- and long-term scheduling strategic lead on high profile projects and to assess and respond to urgent operational issues.The individua

Position Summary:This individual is responsible for the compliance review of Biopharmaceutical GMP data. This includes the review and approval of in-process release and stability test data. Provides QA oversight of analytical and microbial laboratory activities including but not limit

Position Summary:This individual is responsible for the compliance review of Biopharmaceutical GMP data. This includes the review and approval of in-process release and stability test data. Provides QA oversight of analytical and microbial laboratory activities including but not limit

This role contains the following responsibilities covering 2nd shift hours (2:00 pm through 10:30 pm) Monday through Friday:Position Summary:The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. The core fun

This role contains the following responsibilities covering 2nd shift hours (2:00 pm through 10:30 pm) Monday through Friday:Position Summary:The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. The core fun

This position supports the Facilities team which includes Maintenance and Metrology. Primary responsibilities will be for the administration of the Computerized Maintenance Management System (CMMS). This includes but is not limited to establishing workflows to build the asset database

This position supports the Facilities team which includes Maintenance and Metrology. Primary responsibilities will be for the administration of the Computerized Maintenance Management System (CMMS). This includes but is not limited to establishing workflows to build the asset database

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

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