This position is a fantastic opportunity to join a leading clinical research organisation, working across all phases of clinical development. In this role, you will lead the QA department; overseeing team members as well as the processes and operations of the division. The ideal candidate will have a significant QA profile in the pharma, CRO or biotech world - 10+ years' experience in working with GCP regulations, managing audits and QA documentation i.e. CAPAs, validation and EU directives.
Salary & Benefits:
Up to £80k + benefits and bonus scheme
Role and responsibilities:
*Lead the QA department - line management of personnel and management of operations
*Manage internal and external audits and site/vendor inspections or investigations
*Manage training across the company for QA related activities
*Take control of CAPA programme, managing data analysis and continuous improvement
*Lead sponsor audits
*Represent QA in bid defences, governance activity and project meetings
*Collaboration externally with sponsors and clients
Requires skills and qualifications:
*Bachelor's Degree - Life Science discipline preferred
*Several (8-10) years' experience within QA in clinical research, pharma, biotech or CRO environment
*Managerial experience - previous line management desired
*Strong working knowledge of GCP and EU directives
In this role you'll be joining a world leading organisation, making a difference to thousands of people worldwide. You will be able to grow and develop your career potential, as well as having access to world-class resources, a team of highly skilled and motivated colleagues and excellent training programmes.
To apply for this position and put yourself under immediate consideration, send your CV to john.spring@secpharma.com or call +44 (0) 207 255 6650
