Quality Specialist/Quality Auditor
Our client has an exciting opportunity for an experienced QA professional to join their Global Development Quality group as a contract Quality Specialist. This role offers the opportunity to work for a thriving and growing organisation located in Moorgate, London. The position is initially a 6 month temporary contract role, with the potential to extend and our client offers hybrid working (1 - 2 days per week in the office). The hourly rate for this assignment is between £15.65 - £22.00 per hour (maybe have some flexibility depending on experience), plus 25 days holiday pro rata.
This role will expose you to the full range of investigational medicinal products in the organisations 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.
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.