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Senior Clinical Manufacturing Associate - Downstream
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- We share a passion for seeking gene therapy cures for devastating diseases and making a difference for patients.
- As a Senior Clinical Manufacturing Associate, you will be part of a team responsible for the cGMP manufacture of viral vector therapies for use in clinical trials.
- Additional responsibilities include set-up, operation and cleaning of equipment, equipment and process monitoring and troubleshooting, ordering and receiving materials, authoring technical documents, training and mentoring junior staff, leading quality and process improvement projects, ensuring cGMP equipment and manufacturing area are in a safe and audit-ready state, and collaborating with functions supporting cGMP manufacture.
- The ideal candidate will also have a strong passion and curiosity for science and gene therapy with the desire to contribute individually and collectively in a dynamic, fast-paced environment.
- Manufacturing processes include, but are not limited to: cell line initiation (vial thaw), cell line scale-up, bioreactor operations, transfection, harvest clarification, TFF, column packing, chromatography and bulk drug substance fill
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