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Role: Quality Auditor
Location: Hybrid / London (EC2M 6UR) 1 day per week on-site
Duration: 6 Months
Rate: Up to 26/hour PAYE
This role will expose you to the full range of investigational medicinal products in the 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. We are therefore looking for excellent communication skills, an ability to manage issue resolution, confidence to work with minimal supervision, and a keen eye for detail.
Experience:
Experience should be in the pharmaceutical/chemical industry or government drug-regulatory agency with a working knowledge of cGMP regulations. Effective communications (oral/written) and interpersonal skills are necessary.
Qualification:
Ideally you should have existing experience in a QA or similar role in a GMP environment, however we would be just as interested in new science graduates (Bachelor's degree minimum) with the right attitude and a willingness to learn.
To apply, please submit your CVs in the first instance
