GCP Associate Director – 10568
A great opportunity to work full time for a recognized diagnostic and global clinical trial testing service based in North UK
My client is keen to employ someone who will be responsible for establishing a strong Quality culture and recruit into a team of professionals within a GCP environment
Manage all aspects of quality assurance including audit/inspection process, Quality Inspection (QI) tracking, and Corrective Action & Preventative Action (CAPA) process. Lead large scale projects that drive quality throughout the organization. Liaise with clients and regulatory bodies to ensure we meet and exceed expectations.
Support the operation in process improvement initiatives; develop Standard Operating Procedures (SOPs) to support the Quality Management System (QMS). Develop, implement and report Key Performance Indicators (KPIs).
Lead a team of quality assurance professionals that partner strategically with site leadership to promote and support an ‘audit-ready, all the time’ culture.
Qualifications and Experience
Bachelor’s degree required.
7 years of experience in quality assurance required; experience in a laboratory, pharmaceutical or clinical research setting preferred.
3 years in progressive leadership experience required; experience managing global quality assurance and/or regulatory affairs preferred.
Knowledge of and demonstrated experience in Good Clinical Practice (GCP), ISO15189, NEQAS, CAP, CLIA strongly preferred.
You will receive from this role:
An opportunity to travel across other sites
Excellent support structure
Please send your CV to Steven.firstname.lastname@example.org or call on +44 333 5 777 578