Reference Number: JO-2008-453252
Qualified Person (IMP)
Job Type: Permanent
Qualified Person (QP)
A leading early phase contract research organisation based in central London are looking to bring on board a Qualified Person. This business conducts clinical trials on a multitude of volunteer panels in order to develop new medicines, treatments and cures for the future, helping to improve the quality of life for others.
As a Qualified Person you will be responsible for assuring batches of medicinal products have been manufactured and assembled in compliance with the GMP legislation as well as assisting in the maintenance of the companys quality management systems and first class standard operating procedures.
You will work closely with the Principal Investigator, Research Physicians, Project Managers and other core members of the clinical project team to ensure safe and efficient conduct of clinical trials. This role will offer you an excellent opportunity to further your experience in clinical research and regulatory matters.
Registered QP, eligible to be included on a manufacturing licence for investigational medicinal products (IMPs)
Strong Quality Assurance/ Control and Quality Systems background
Demonstrable experience of Good Manufacturing Practice (GMP) and regulatory standards (MHRA, EMA) within a pharmaceutical manufacturing and clinical trials environment
Proven experience of managing multiple work streams, able to manage and self-prioritise
Involvement and assistance with planning, conduct, reporting and follow up of GMP audits/ inspections
If this sounds like an ideal next step please apply online. Any queries can be directed to Kimberley Warren on 07900981267.