Vice President, Site Leader, Cell Therapy Manufacturing - Bothell

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. Lead the company's Cell Therapy Drug Product commercial/clinical manufacturing facility in Bothell, Washington and associated operations. · ...

Lead the company's Cell Therapy Drug Product commercial/clinical manufacturing facility in Bothell, Washington. · Accountable for manufacturing operations, overall site budget and cost optimization, · talent management/succession planning including hiring, training, · and develop ...

This position collaborates on project efforts with site and global stakeholders across manufacturing, quality, supply chain, information technology, facilities, manufacturing science & technology, and other functional areas. · Bachelor's degree in engineering, science, informatio ...

Cell therapy is one of the most exciting new forms of cancer treatments being studied today. · Lead project planning activities including development of a project schedule. · Identify stakeholders and drive conversations to align on clear project requirements scope and deliverabl ...

Plans and schedules production related activities at the cell therapy manufacturing facility. · ...

The Quality Engineering team at Juno is responsible for providing Quality Assurance oversight of environmental validation and engineering documents. The position of QA Specialist - Environmental Oversight reports to the Manager, Quality Engineering. · Provide oversight of cleanro ...

We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. · ...

The individual in this role will be responsible for supporting the ongoing operations of the Manufacturing, Science and Technology (MSAT) team within the manufacturing site. · ...

The incumbent is responsible for supporting the operations in our cGMP clinical manufacturing site producing plasmids, viral vectors, and autologous cell therapies. · This role executes manufacturing operations safely, adheres to cGMP and SOPs. · ...

The incumbent supports operations in our cGMP clinical manufacturing site producing plasmids,viral vectors,and autologous cell therapies · ...

+The incumbent is responsible for leading and overseeing day-to-day Quality Assurance (QA) operations for the LyFE manufacturing facility, including leadership for the QA team. · +Responsible for supporting Quality oversight of GMP operations at the manufacturing facility and ens ...

The Manager of Patient Scheduling will serve as a key member of Patient Operations in the Supply Chain organization. · This individual will be responsible for managing all operations regarding the collection and management of patient cells during the cell therapy process. · ...

The incumbent is responsible for supporting the operations in our cGMP clinical manufacturing site producing plasmids, viral vectors and autologous cell therapies. · ...

The Manager, Patient Cell Operations is a key member of the Patient Cell Supply Chain team within the Supply Chain organization. This role is responsible for the operational oversight and management of patient cells throughout the cell-therapy lifecycle, including apheresis, tiss ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Synkriom, is seeking the following. Apply via Dice today · JOB DESCRIPTION: · The Material Handler is responsible for supporting warehouse operations within a cGMP-regulated biolo ...

+Job summary · The incumbent is responsible for Ocellos (Trakcel) and Binocs applications that support technical and clinical operations. This role supports patient operations, supply chain, manufacturing and quality teams. · +ResponsibilitiesResponsible for the overall budget ma ...

The role of Associate Director involves leading project plans from ideation to execution. Key responsibilities include developing project communications for peers and senior stakeholders, · Preparing co-ordinating and leading cross-functional workshops. · Drive tracking actions d ...

The incumbent is responsible for supporting the operations in our cGMP clinical manufacturing site producing plasmids, · viral vectors and autologous cell therapies.This role works closely with Manufacturing Operations, Quality Control, · Quality Assurance, and Supply Chain to es ...

Challenging. Meaningful. Life-changing. · Associate or bachelor's degree in related field preferred · ...

The Quality Associate position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (JuMP). The primary focus of the QA Associate role will be to support routine clinical and commercial production to ensure consistent compliance with regu ...