Qualified Person

Responsibilities include:

* Organise and provide QP certification for pharmaceutical products (Commercial and Investigational medicinal products)
* To support the Director of Quality in interactions withUKand International regulatory bodies, taking an active part in hosting inspections.
* To ensure GMP compliance across the Services Organisation by:
* making regular visits to operational departments and offering advice and guidance with respect to regulatory expectations and recognised best practice
* Supporting Line QA staff in their inspection and checking duties as required
* Providing training to staff to increase understanding of the regulatory GMP requirements and implementation of best practices
* Promoting compliance across the site by adherence to, Quality Policies, SOPs and training programmes
* Taking an active part in the self inspection schedule
* To provide advice and guidance to operational groups and clients.

They are looking to offer a great career path for ambitious QPs offering a wide range of Pharmaceutical products and production experience.

If you are interested in this opportunity please email an updated CV to Jade Tetlow Head of Quality Assurance Recruitment. Alternatively call 0207 758 7311 for further information.

Keywords: Quality Assurance, Regulatory Affairs, QA, GxP's, SOPs, Systems, Quality Management, Product Release, GMP, Good Manufacturing Practice, Quality Assurance Manager, Qualified Person, Audit, Auditing, Validation, UK Head of Quality Assurance, Manufacturing, Site Quality Assurance.

To find out more about Real Staffing please visit www.realstaffing.com