A niche provider of drug development services based in the South East are currently looking to hire a new Quality Assurance Manager.
Being responsible for the Quality Department you will look to:
Prepare and distribute SOPs throughout the organisation.
Maintain and update the Quality Management System.
Provide training to members of staff on all elements of GCP.
Co-ordinate plan and conduct internal and external clinical audits.
Support the preparation of regulatory authority inspections in connection with GCP activities, processes and facilities.
Maintain an awareness of regulations and guidelines relating to the conduct of all clinical trials.
To be eligible to apply you must 3-4 years experience in clinical QA and have a strong understanding of the clinical drugs development process, including GMPs and GXPs.
You must have strong abilities in the areas of managing employees, project management and process improvement. You need to be able to self-start, work autonomously with little supervision and be willing to make your mark on the organisation. It is a fantastic opportunity looking to pay up to £50k including benefits.
If you are looking for a new position that will offer a new challenge with a growing clinical trials company please email an updated CV to John Morkus or call 02077587311 for further information.
Keywords: Clinical Trials, GCP, Regulatory Affairs, QA, QC Activities, GMPs, GxPs, SOPs, Systems, Quality Management.
Real Staffing - 2 years ago
Real is a leader in the provision of pharmaceutical & biotechnology, medical devices, public sector, banking & financial services, i...