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 firstname.lastname@example.org 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.
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.
Talaris is searching for an Associate Director, Program Manager to lead one of our exciting programs to commercialization. The position reports to the Head of Program Management and serves as the strategic and operational thought partner to the Program Team Leaders.
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.
The Senior Accounting Analyst will be based in Louisville, KY and reports to the Controller. The Senior Accounting Analyst will work hand in hand with the Controller to continue to improve the financial reporting and compliance processes as well as identify areas of needed improvement across the finance function.
The Materials Management Supervisor, to be based in Louisville, KY reports to the Manager, Supply Chain, is responsible for maintaining sufficient levels of materials for cell therapy manufacturing at Talaris Therapeutics. The Materials Management Supervisor will oversee GMP receiving, shipping, and kitting activities.
Manages and tracks overall operations of a clinical study including project plans, budget, and resource management. Leads development of study operational plans and is able to provide input into other functional area plans as needed. Provides excellent oversight of the CRO, vendors and sites. Ensures compliance with GCP and regulatory guidelines. Position reports to Director, Clinical Operations.