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Position Summary: The Quality Assurance Specialist I/II Manufacturing is responsible for assuring products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems,…
JOB SUMMARY The Director has overall responsibility for the company’s Environmental, Health, Safety, and Sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous…
Position Summary The Senior QA Specialist provides Quality Assurance oversight and support for Facilities, Engineering, Validation, Cleaning Validation, Metrology, computerized systems, and related GMP activities…
This position is on a 2-2-3 shift, Day Shift (6am-6pm) The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing…
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…
JOB SUMMARY General responsibility for the installation, day-to-day 24/7 operation, maintenance, and modification of all KBI Biopharma site systems. This position is also responsible for repairs, troubleshooting,…
Job Summary Senior Director of Quality, Quality Site Head at a contract manufacturer of microbial fermentation and/or mammalian cell culture protein therapeutics. Lead a Quality Assurance and Quality Control team which…
This position is on a 2-2-3 shift Day Shift (6am-6pm) The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug…
*Dayshift: 6AM-6PM, 2-2-3 rotating schedule 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…
*Nightshift: 6PM-6AM, 2-2-3 rotating schedule The Senior Manufacturing Associate I/II (Days) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for…
Build cloud-based data platforms and tools for biopharmaceutical R&D, using Python, JavaScript/TypeScript, React, AWS, and data stacks like Pandas and Airflow to accelerate drug development.
Job Summary The Senior Director, Warehouse Operations is responsible for strategic leadership, operational performance, and continuous improvement of all warehouses, inventory, logistics, warehouse purchases, warehouse…
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…
Manufactures biopharmaceutical products in a cleanroom, operating upstream/downstream bioprocessing equipment and following cGMP procedures overnight.
JOB SUMMARY: General responsibility for the installation, day-to-day 24/7 operation, maintenance, and modification of all KBI Biopharma site systems. This position is also responsible for repairs, troubleshooting,…
Lead biologics manufacturing science and tech-transfer at a cGMP site, overseeing process validation, tech transfer, and cross-functional teams to scale production and ensure regulatory compliance.
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…
This is a remote role with preference for candidates located on the West Coast, USA. Position Summary: Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and…
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…
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