KBI Biopharma Jobs in United States

We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. · ...

Responsible for performing, managing and tracking deliverables for batch disposition to include compiling batch and batch linked documentation required for final and conditional product release. · ...

The Materials Coordinator manages all activities related to the planning,purchase,receipt,warehousing,and distribution of supplies and materials used in the companys development,production,and administrative support functions. · High School Diploma with 2 years experience in ware ...

/h2/b/Job summary//b/h2/p/The Manufacturing Associate I will perform Upstream or Downstream production activities for early /a>and late-phase Cell Culture programs in a GMP environment./p/p,/h2/b/Responsibilities:/b/h2/ul/li-Manufacture cell culture products according to manufact ...

The Manufacturing Support Associate I/II position is designed as an introduction to the environment of cGMP manufacturing. · Performs and Maintains Manufacturing facilities by routine/nonroutine cleanings. · Cleans, operates and maintains the Process Waste area. · ...

Able to manage a project team within Program Management, ensures project and business management is executed appropriately within the team. · ...

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. · Executes routine Microbial Laboratory work. · Ma ...

Position Summary: · This position is on a 2-2-3 shift, 6a-6p. The Manufacturing Associate I/II – Downstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment.  · The Manufacturing Associate I/II – Dow ...

Job Description · Job Description · The Manufacturing Associate I 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/GDP/GLP stan ...

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 innova ...

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 innova ...

*This is a hybrid role with the option to work two days a week from home* · About this job: · Join KBI Biopharma's 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. T ...

JOB SUMMARY: · The Manufacturing Quality Assurance (MQA) Supervisor is responsible for supervising the MQA team who supports the Manufacturing Process and Areas as part of a GMP Contract Manufacturing Organization. MQA Supervisors are expected to provide sound guidance to MQA tea ...

Job Title · Global Material Planner Senior at KBI-Biopharma · Manage end-to-end aspects of material readiness of assigned projects to enable timely GxP production at KBI's global facilities operations. · This Includes: · Bulk Product Management · Purchase Requisition ( ...

The Supply Chain Inventory Analyst is responsible for managing assigned inventories through daily, weekly, monthly and annual physical counts. · ...

This position is responsible for the installation maintenance and modification of all site systems including repairs troubleshooting corrective and preventative maintenance of associated systems and equipment. · ...

The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. · In-process, characterization, stability,and/or release testing as assigned. · Execution of method transfer method qualification and/or method vali ...

The Manufacturing Support supervisor leads a team of manufacturing associates to perform upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. · ...

JOB SUMMARY The Associate Manufacturing Specialist/Manufacturing Specialist I, II, III/Sr. Manufacturing Specialist, Manufacturing Technical Support and Investigations (Manufacturing Specialist) is responsible for supporting equipment and cGMP operations for the upstream, downstr ...

JOB SUMMARY : The CMF Manufacturing Assistant position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non-routine cleanings and maintains gowning supplies for the locker rooms and gowning rooms at the CMF GMP facility to s ...