Overview
Join Us in Changing Lives
At OXB, our people are at the heart of everything we do. We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
We’re currently recruiting for a 12-month, Quality Control Team Lead to lead a team of Scientists, effectively coordinate the daily activities to ensure timelines are met whilst maintaining compliance with GMP & safety regulations.
Responsibilities
* Provide line management and leadership to a team of analytical scientists and technicians, including performance management, motivation, and recruitment.
* Coordinate day-to-day laboratory activities in collaboration with fellow team leaders and the scheduling team to ensure smooth workflow and delivery.
* Perform, review, and approve analytical assays for QC release and stability in full compliance with GMP requirements.
* Plan, deliver, and evaluate training programs; review and approve associated training documentation.
* Lead or contribute to troubleshooting activities, technical investigations, and process improvements.
* Drive and support departmental and cross-functional initiatives and projects to enhance quality and efficiency.
* Complete quality documentation, including QIs, deviations, CAPAs, and change controls, accurately and within required timelines.
* Write, review, and maintain ASG policies, SOPs, and related documentation to ensure alignment with regulatory standards.
* Ensure laboratory operations and equipment remain in a state of GMP compliance and audit readiness.
* Represent the department during customer and regulatory inspections and actively participate in customer meetings.
Qualifications
* BSc Degree in a relevant Scientific discipline
* Laboratory technical experience in one or more of the following areas: cell culture, qPCR or ELISA
* Ability to work within GMP regulations and maintain compliance; previous experience of working within a GMP environment
* Line management skills are desirable
* Good time management skills and ability to prioritise
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.
Why Join Us?
* 💸 Competitive total reward packages
* 🧘 Wellbeing programmes that support your mental and physical health
* 🚀 Career development opportunities to help you grow and thrive
* 🤝 Supportive, inclusive, and collaborative culture
* 🧪 State-of-the-art labs and manufacturing facilities
* 🌍 A company that lives its values: Responsible, Responsive, Resilient, Respect
We want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together—through passion, commitment, and teamwork.
Ready to Make a Difference?
Collaborate. Contribute. Change lives.
We offer:
Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.
Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patient’s cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients’ cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).
Oxford Biomedica 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. Oxford Biomedica’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.
#J-18808-Ljbffr