As a result of growth we are increasing our manufacturing and development capabilities which include the addition of new sites, equipment and processes. We are therefore able to offer opportunities to a Senior MSAT Scientist with a strong process engineering expertise to join our team.
Oxford BioMedica is a pioneer of gene and cell therapy and our work is helping to deliver life changing treatments.
Gene and cell therapy is the treatment of disease by the delivery of therapeutic DNA into a patient’s cells, providing long term and potentially curative treatments for a wide range of diseases. With the potential to transform medicine, the sector holds significant promise with the first commercial products now launched and others rapidly approaching the market
To manage the effective performance of a major project with a tactical focus on meeting the scientific, clinical, manufacturing and business requirements of the department in line with company goals.
Provide technical and scientific support to the clinical and commercial manufacturing activities at Oxford BioMedica (OXB) and third party CMO sites including technology transfer, technical troubleshooting, complex deviation investigations, change control, and continuous improvement.
As necessary lead and perform root cause investigations using a systematic approach to resolve complex problems and lead multidisciplinary teams in developing and implementing solutions.
Partnering with other functions to ensure scale-up is robust and scientifically sound leading to consistent performance
Key responsibilities and accountabilities:
The candidate will be an influential MSAT representative within OXB working across multiple projects at different stages of the commercial product lifecycle.
Provide technical expertise to other departments and contribute to the scientific and business needs of the company.
Provide leadership and direction on MSAT activities to the various in-house and partnered project teams to ensure all project deliverables and milestones are met within agreed scope, timelines and budget
Responsible for internal documentation to ensure quality and compliance required for regulatory submissions.