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A leading company in viral vector CDMO is seeking a Sample Coordinator to support laboratory activities. The role involves managing samples, coordinating requests, and ensuring accurate record-keeping. Ideal candidates are organized, detail-oriented, and have a genuine interest in science. Join a dynamic team dedicated to delivering life-changing therapies.
Job description:
We want you to feel inspired every day. We’re future-focused, and our business is growing. We succeed together through passion, commitment, and teamwork, and so can you.
We are currently recruiting for a Sample Coordinator to join the Process Development team. The purpose of this role is to provide essential laboratory activities and services supporting the high-quality scientific work conducted at OXB.
Process Development (PD) is responsible for developing world-class viral vector manufacturing processes for Oxford Biomedica’s proprietary products and partnered programmes. PD plays a crucial technical role in Oxford Biomedica’s mission to deliver life-changing gene therapies to patients.
Your responsibilities in this role would be:
Profile description:
About Us:
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life-changing therapies to patients worldwide. As pioneers in cell and gene therapy, we have over 25 years of experience in viral vectors, powering the majority of gene therapies.
We collaborate with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV), and adenoviral vectors. Our capabilities span from early-stage development to commercialization, supported by robust quality systems, analytical methods, and regulatory expertise.
What’s in it for you:
Collaborate. Contribute. Change lives.
Oxford Biomedica is a leading viral vector CDMO dedicated to enabling life-changing therapies. Our expertise in cell and gene therapy involves delivering genetic material via engineered viral vectors, either directly or through modified cells, for the treatment of diseases.