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Oxford Biomedica (UK) Limited in the United Kingdom is seeking a GMP Support Assistant to help maintain clean and compliant manufacturing environments. You will perform routine cleaning and sanitisation of work areas, support the movement of equipment and materials, and assist with stock and inventory control.
You will ensure accurate documentation, follow site procedures, and uphold health and safety standards to support compliant operations within the manufacturing support team.
Carry out routine cleaning and sanitisation of work areas, equipment and materials, to maintain the highest standards of cleanliness and hygiene. Work as part of a team to ensure daily tasks are completed on schedule, helping the facility run smoothly and efficiently. Support the movement and organisation of equipment, consumables and materials throughout the facility, ensuring the right items are available when needed. Assist with stock management activities, including monitoring inventory levels and maintaining accurate records. Complete documentation and records accurately, with a strong focus on attention to detail and compliance. Follow all health, safety and site procedures to ensure work is completed safely and in line with regulatory requirements.
Please note: Our vacancies are typically advertised for a minimum of 10 working days. Once a vacancy closes, it may take a few days for us to provide an update while our Talent Acquisition team and Hiring managers review all applications. Every application is reviewed manually by our recruitment team and hiring managers. We do not use AI to screen CVs or make shortlisting decisions.
No previous experience in Advanced Therapies, manufacturing or pharmaceuticals is required. We are looking for people with the right attitude, strong work ethic and a willingness to learn. You may be working in hospitality, catering, retail, cleaning, warehousing, customer service or another fast-paced environment and be looking for a new career opportunity. To be successful, you’ll demonstrate: Good time management skills and the ability to follow procedures and complete tasks on schedule. A willingness to learn and commitment to personal development. Excellent attention to detail and a focus on maintaining high standards. The ability to work in a structured environment and follow processes accurately. GCSEs (or equivalent) and/or relevant work experience.
OXB 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, OXB has more than 30 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 patients 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). 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.
Job description: Join Us in Changing Lives AtOXB, 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 were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful. We’re currently recruiting for a GMP Support Assistant to join our Manufacturing Support team. In this role, you will ensure GMP compliance through regular cleaning, material transfer and waste removal, playing a key part in advancing our mission and making a real difference.
OXB is a global quality and innovation-led contract development and manufacturing organisation (CDMO) in cell and gene therapy 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, OXB has 30 years of experience in viral vectors; the driving force behind the majority of cell and gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno‑associated virus (AAV), adenovirus and other viral vector types. OXBs world‑class capabilities range from early‑stage development to commercialisation. These capabilities are supported by robust quality‑assurance systems, analytical methods and depth of regulatory expertise.
OXB, a FTSE250 and FTSE4Good constituent, is headquartered in Oxford, UK. It has development and manufacturing facilities across Oxfordshire, UK, Lyon and Strasbourg, France, Bedford MA, and Durham NC, US.
We want you to feel inspired every day. At OXB, were 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 patients 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.
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.