Job Openings

Join the Excitement at AVROBIO

Transformative gene therapies offer the potential to cure.
Come join us in the gene revolution at AVROBIO.

In this role you will be responsible for quality oversight of external GMP Quality Operations and support for clinical-stage lentiviral-based gene therapies. The individual will be responsible for supporting our internal team, responsible for overseeing a network of global contract manufacturers and providing GMP Quality oversight both internally and externally. Key Responsibilities: Provide subject matter …

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Cambridge, MA
Posted 2 days ago

We are seeking a highly motivated, detail-oriented and experienced Senior Accountant to join our growing, progressive, fast-paced Finance team. Reporting to the Assistant Controller, the Senior Accountant will help to ensure that high-quality financial information is created and used to drive decisions in this highly entrepreneurial, clinical-stage biotech company. The ideal candidate for this role …

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The Preclinical Research Operations and Facilities Manager is responsible for the coordination and administration ofAVROBIO’s Laboratoryand internal non-GLP research activities in collaboration with AVROBIO’s researchers to support the discovery stage development programs for lentiviral-based gene therapies focusing on rare diseases, where a faulty gene results in a lack of an essential enzyme or protein. The …

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The Associate Director of  Manufacturing  will  support manufacturing activities related to its ex-vivo gene therapy programs. The candidate is expected to have in-depth knowledge in the field of cell and gene therapy along with direct experience in current manufacturing processes, and will work in a team setting to oversee multiple functions of CMOs working with AVROBIO. …

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Cambridge, MA
Posted 1 week ago

This position will interact closely with R&D gene therapy scientists across the entire preclinical portfolio. Leverage your laboratory bioassay knowledge and/or experience to assist in the preparation, tracking, approval, and finalization of contracts related to ongoing bioassay work occurring at our external CROs. Track contract lifecycles and their associated output. Obtain purchase orders, and log …

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Cambridge, MA
Posted 3 weeks ago

As Contracts Administrator in the Legal Department, you will be assisting all areas of our gene therapy business by providing contract support as described below.  This position will report to the Associate Director, Contracts. Key Responsibilities: Manage intake of contract requests using Legal Department’s contract management system, routing requests to appropriate personnel. Monitor contract requests …

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Cambridge, MA
Posted 3 weeks ago

AVROBIO is seeking a highly-motivated individual to provide program management support for one or more gene therapy programs. This person will work collaboratively within the program teams to integrate diverse R&D activities including, but not limited to, preclinical research, clinical development, manufacturing, regulatory affairs, commercial and finance. This is an exciting opportunity for a qualified …

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Cambridge, MA
Posted 3 weeks ago

AVROBIO is seeking a highly motivated individual with strong leadership and program management skills to oversee one or more gene therapy programs in AVROBIO’s pipeline ranging from preclinical to clinical stages of development. The Program Leader will work collaboratively to manage and integrate diverse R&D activities including, but not limited to, preclinical research, clinical development, …

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Cambridge, MA
Posted 4 weeks ago

AVROBIO, Inc. is seeking an exceptional, energetic, business-minded corporate attorney with demonstrated securities law experience advising publicly traded biotechnology or pharmaceutical companies in a law firm or in an in-house legal environment.  Reporting to the General Counsel, this individual will be the second lawyer at an exciting, fast-growing and innovative gene therapy company headquartered in …

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Cambridge, MA
Posted 2 months ago

The Senior Manager, Quality Compliance is responsible for providing compliance guidance and support for clinical-stage lentiviral-based gene therapies.  The individual will be responsible for ensuring quality systems (including internal/external audits, vendor management, deviations / CAPA management, and change management) while driving compliance with applicable guidelines and regulations. Key Responsibilities: Responsible for compliance with applicable corporate …

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Cambridge, MA
Posted 2 months ago

Understanding the behavior and fate of genetically-engineered cells is crucial for improving the safety and efficacy of gene therapy. Statistical and mathematical models are vital for extrapolating relevant information from high throughput sequencing data. This role is specifically designed to address questions on how best to optimize gene therapy platforms at basic and translational levels. …

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Cambridge, MA
Posted 2 months ago

We are looking for a motivated, flexible, creative and energetic team member to join our Pompe team within our R&D Preclinical Department.  You will be involved in the field of ex vivo lentiviral vector gene transfer into hematopoietic stem/progenitor cells with a mission of curing lysosomal storage disorders and rare diseases in one dose.  Perform …

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