Quality Specialist

Our global pharmaceutical client based in London has an exciting opportunity for an experienced QA professional to join their Global Development Quality group as a contract Quality Specialist. This role will expose you to the full range of investigational medicinal products in the company development pipeline, from simple small molecules through to complex immunotherapy treatments, and a chance to make a real difference to patients receiving these lifesaving and life changing medicines. The position is a temporary contract initially signed off for 6 months with a possible extension, offering an hourly rate of £15.65 - £26.61 depending on experience, plus holiday pay and other benefits. The successful candidate will be required to work full-time hours (37.5 hours per week Monday – Friday) and our client offers the option of hybrid working. As a Quality Specialist, you will be responsible for the final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings. The compilation and approval of this data pack and presentation to the QP for final release is the core function of the role, and you will work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally around the world to help you achieve this. Our client is therefore looking for excellent communication skills, an ability to manage issue resolution, confidence to work with minimal supervision, and a keen eye for detail. Ideally you should have existing experience in a QA or similar role in a GMP environment, however our client would be just as interested in new science graduates (Bachelor’s degree minimum) with the right attitude and a willingness to learn. Qualifications New science graduate (Bachelor’s degree minimum)