What are the responsibilities and job description for the Co-op, External Manufacturing position at Vor Bio Co-ops?
We create shielded stem cell transplants that enable targeted therapies to attack only cancer cells
Every year, thousands of patients with Acute Myeloid Leukemia (AML) and other blood cancers relapse post-transplant with no safe and effective treatment options. Vor Bio's approach provides the first opportunity to deliver potentially curative treatments post-transplant.
Our novel platform creates a shielded stem cell transplant that is designed to enable multiple modalities and therapies, including Antibody Drug Conjugates (ADCs) and Chimeric Antigen Receptor T (CAR-T) cells, which could potentially be effective against the tumor, but are toxic to normal cells. Vor's genetically engineered transplant provides a protective shield to the healthy cells and thereby allows the cancer cells to be specifically targeted for destruction.
By shielding healthy cells, Vor Bio is aiming to potentially cure Acute Myeloid Leukemia (AML) and other blood cancers. Come be a part of a passionate team striving to collaboratively develop a groundbreaking approach to cancer treatment, one of medicine's greatest challenges.
What we value in our fellow Voracians
Passion : Enthusiastically driving our science toward innovative medicines
Fellowship : Fostering genuine bonds of collaboration and mentorship
Humility : Acting selflessly by putting the collective mission first
Who we are looking for :
Vor Bio is seeking a highly motivated and detail-oriented Co-op student to join our External Manufacturing team. As a key team member, you will play a critical role in supporting the manufacturing of our innovative clinical products. This team is responsible for ensuring the scalability, efficiency, and robustness of manufacturing processes. It bridges the gap between process development and clinical manufacturing by optimizing cell therapy processes, troubleshooting issues, and ensuring compliance with regulatory standards.
Key areas of responsibility :
- Manage and analyze critical data related to clinical manufacturing results and process trending
- Collaborate with internal and external manufacturing teams to support clinical product production
- Assist in investigations, deviations, and CAPA closure and reconciliation
- Track and trend quality events to drive internal manufacturing excellence
- Draft and revise SOPs and Manufacturing Batch Records for continuous improvement
- Work closely with cross-functional teams, including Process and Analytical Development, Manufacturing, Supply Chain, Quality Assurance, and Quality Control
Qualifications :
LI-DNI
