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An established industry player in cell and gene therapy is seeking a motivated Sample Management Coordinator to join their Quality Control team. This exciting role involves managing samples from receipt to shipment, ensuring quality control and compliance in a highly regulated environment. You will collaborate with cross-functional teams, author SOPs, and maintain meticulous records. The company values innovation and teamwork, offering a supportive and inclusive workplace where your contributions can make a real difference in delivering life-changing therapies. If you're passionate about science and eager to grow in a dynamic environment, this opportunity is for you.
Job description:
We are at the centre of the rapidly growing cell and gene therapy sector. We deliver life-changing therapies to patients, and so can you.
We are currently able to offer an opportunity for a motivated individual with an interest in science to join us as a Sample Management Coordinator 2 within our Quality Control (QC) team. The purpose of this role is to receive, store, issue, pack, ship, organise and dispose of samples in a controlled manner.
Our QC team supports the development of products through analytical testing to facilitate manufacturing, shelf life setting and process development, ensuring appropriate quality controls and use of analytics.
Your responsibilities in this role would be:
We are looking for:
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 around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies.
OXB collaborates 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. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
What’s in it for you:
Collaborate. Contribute. Change lives
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