Accenian are excited to be working with a Biopharmaceutical company developing T-cell therapies in Oncology seeking a Senior QA Specialist to join the team.
You will have sole responsibility for the GMP activities and need to have over 5 years relevant experience working in a QA role, with direct responsibility for maintaining GMP standards.
You need to have worked as a line manager for at least 3 years in a quality setting and experience with MHRA (E) and HTA (P) inspections.
You must:
• Hold a BSc or MSc in pharmaceutical sciences and have had training to become a QP. • Worked with validated paperless documentation and batch review systems. • Have an understanding of CAR T cell technology • Lead Audits and host inspections and audits. • Project design and project management.
If you are interested in applying for this role, please send your CV to [email protected]