Title: Qualified Person (QP) Location: North East of England Employment Type: Contract Salary: Highly competitive day rate, depending on experience I am currently working with a very well established organisation, which leads technical innovations across the UK in different scientific sectors including pharmaceuticals and biologics. We are currently looking for a contract QP (ideally with experience of IMPs), who can be a named QP on the MIA, and manage the QMS, along with overseeing the release of products. The main duties and responsibilities: To review/release Batch Manufacturing Documents to ensure compliance with EU GMP and / or the Product Specification File/marketing authorisation (or other where relevant). Ensure continued compliance, operationally, to site licences for Investigational Medicinal Products and unlicensed medicines manufactured, and act as a key contact for the MHRA & Home Office. To observe and actively promote Good Manufacturing Practice (GMP) as per company procedures. Experience required: Fully qualified QP, ideally across IMPs. Experience of releasing vaccines, small molecules and/or Biologics experience. Knowledge of global regulations, and experience of dealing with the MHRA. Interested? Or know someone who will be? SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.