Careers

at Talaris

Careers

Talaris is hiring!  We are an equal-opportunity employer offering competitive benefits and a mission-driven culture that focuses on improving outcomes for the patients we serve.  Our open positions are listed below:

To apply, please send your CV to careers@talaristx.com with the position you are applying for in the subject line.

If the position you are looking for is not listed, please check back frequently for new open positions, as our team is growing rapidly.

Materials Management Technician

The Materials Management Technician is responsible for day-to-day operations related to material receipt and disposition to support clinical cell therapy manufacturing in a GMP facility. The primary responsibilities of this role focus on material receipt and disposition, shipping, and kitting activities.

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Research Assistant, Research and Development

A Research Assistant, to be based in Louisville, KY is responsible for supporting analytical sample testing related to the research and development of novel cell therapy products under the supervision of a Senior Scientist for preclinical and clinical research and development as well as day-to-day operations related programmatic organization activities.

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Cell Processing Associate I, Manufacturing Operations

A Cell Processing Associate I, to be based in Louisville, KY is a production professional responsible for the day-to-day operations related to clinical cell therapy manufacturing in a GMP and GTP compliant ISO 7 classified cleanroom facility.

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Procurement Specialist

The Procurement Specialist is responsible for procurement of materials for GMP operations, negotiating and managing supplier agreements, and maintaining supplier relationships at Talaris Therapeutics. This position will seek to reduce the cost of materials while adhering to the quality management system.

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QA Document Specialist

The QA Document Specialist is responsible for maintaining and sustaining change control, training and documentation processes. Supports departments by creating, processing, distributing and controlling revisions of the quality system and related documentation.

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