Share your **integrity** with us by helping to ensure compliance across our processes.
Oxford Biomedicas Manufacturing Team is responsible for the production and aseptic fill and finish of vectors, for our clients and partners, to GMP standard.
We are looking for a motivated & creative GMP specialist interested in using their knowledge to author and co-ordinate our manufacturing documentation. You may off already have some SOP writing experience or similar or perhaps looking to move into this type of career, either way we would be like to hear from you.
**Your responsibilities in this role would be:**
* Authoring of clear and concise GMP documentation to support manufacturing of clinical and commercial grade lentiviral vectors * Co-ordinating the document updates and reviews with other departments in order to ensure project time lines are achieved with minimal disruption to other activities within the facility * Ensuring of adherence to manufacturing schedules to allow for timely availability of the batch manufacturing records. * Working with the Senior Technical Writer to improve GMP documentation to minimise errors * Work effectively alongside manufacturing teams and process compliance to ensure documentation is delivered in a timely manner
**To be successful in this role, you will have the following skills and experience:**
* Graduate in a science based subject, and/or experience of working to GMP standard within an aseptic manufacturing environment * Competent user of MS Office applications * Maintain up-to-date knowledge of manufacturing processes and procedures * Experience of authoring clear and concise GMP documentation such as SOPs or Batch Manufacturing Records (BMRs). * Knowledge of GMP and regulatory documentation requirements * Past experience working within a GMP manufacturing facility is beneficial.