I'm currently looking for a Quality Manager to join an exciting Cell & Gene Therapy manufacturing business based in the London area. As the Quality Manager, you're role will be varied, however you will also be responsible for the following:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Manager will be varied however, the key duties and responsibilities are as follows:
Ensuring all QA activities related to the manufacture, testing and release of cell and gene based products meet the required standards.
Manage the daily activities of the Quality Management System, including deviations, CAPA's and change controls.
Review and sign off of batch manufacturing records and associated documentation to prepare for the release of ATMP's and IMP's to GMP required regulations.
Work cross functionally across the departments to develop strong relationships and advise on Quality related issues, training and development.
To be successful in your application to this exciting opportunity as the Quality Manager we are looking to identify the following on your profile and history:
1. Relevant degree within a Scientific Discipline.
2. Proven industry experience managing Quality Management Systems, e.g. Deviations or Change Controls
3. A working knowledge and practical experience within an ATMP or Cell & Gene Therapy, GMP Quality position.
Key Words: Quality Manager, GMP, Viral Vector, ATMP, Quality Management System, QMS, Quality Leadership
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.