BT

BlueRock Therapeutics

Verified Job Source

Striving to transform the treatment of disease by harnessing the power of cell therapy

Cambridge, Massachusetts

Biotechnology Research
201–500 people

About

BlueRock Therapeutics is a clinical stage cell therapy company focused on creating cellular medicines to treat devastating diseases. We are harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investigational cell therapies, one for the treatment of Parkinson’s disease and one for the treatment of primary photoreceptor diseases, are clinical stage programs. BlueRock was founded in 2016 as a joint venture of Versant Ventures and Leaps by Bayer, the impact investing arm of Bayer AG that invests in paradigm-shifting breakthrough innovation. In late 2019, BlueRock became a wholly owned, independently operated subsidiary of Bayer AG. Our culture is defined by the courage to persist regardless of the challenge, the urgency to transform medicine and deliver hope, integrity guided by mission, and community-mindedness with the understanding that we are all part of something bigger than ourselves. For more information, visit www.bluerocktx.com.

Open positions

Senior Analyst, Analytical and Quality Control

On-site · Toronto

The Senior Analyst supports GMP testing for cell-based therapeutics, focusing on flow cytometry and cell-based assays for release and compliance. They are also responsible for writing and reviewing SOPs and coordinating quality control functions for laboratory and cleanroom operations.

Analyst II, Analytical and Quality Control

On-site · Toronto

The Analyst II supports QC testing for cell-based therapeutics in a GMP compliant manner, covering raw materials through to final drug products. Responsibilities include writing SOPs, managing laboratory operations, and coordinating with CROs for external testing.

Senior Analyst, Analytical and Quality Control

On-site · Toronto

The Senior Analyst supports A&QC compliance by managing quality records, deviations, and CAPAs within the electronic Quality Management System. They are also responsible for authoring SOPs and ensuring GDP compliance for laboratory records to meet global standards.

Senior Director, MSAT

On-site · Toronto

Lead the MSAT organization to bridge process development with GMP manufacturing and drive the technical startup of a new cell therapy facility in Toronto. Accountable for technology transfers, process monitoring, and the deployment of automation and digital technologies to improve operational efficiency.

Director, Supply Chain

On-site · Toronto

Lead the end-to-end supply chain strategy and operations to support research, clinical manufacturing, and trial execution for cell therapy portfolios. Establish integrated planning, sourcing, and distribution capabilities while overseeing teams responsible for procurement and materials management.

Director, Device Development

Hybrid · Toronto

Lead the end-to-end design, development, and clinical readiness of complex medical devices and combination products for cell therapy portfolios. Provide strategic technical leadership and manage relationships with internal stakeholders and external partners like CDMOs.