Working within the, Quality Assurance and Regulatory Affairs Team you will provide excellent administrative support and be involved in maintaining an effective and controlled documentation system supporting quality & regulatory standards within the business.
This will involve support to ensure the day-to-day management & co-ordination of requests and updates to technical documentation, document filing & archiving and retention, undertaking collation of required reports at necessary timepoints, support technical query requests, along with supporting the maintenance of supplier assessment reviews.
The Regulatory Affairs Administrator will assist, support and participate in the review and issue of Standard Operating Procedures (SOP) and associated documentation and develop the necessary skills to support the investigation and accurate documentation of customer complaints.
They also actively contribute to and support the team in taking notes during meetings and participate with continuous improvement & development of the department. You will be supported to develop skills necessary to assist in maintaining a proactive quality culture throughout the organisation and assist activities to achieve the standards of excellence as set out in the company’s clinical governance, quality, and environmental policies.
The successful candidate must be able to take initiative, solve problems and deliver independently as well as working within a multi-disciplinary team environment, whilst working to a high degree of accuracy.Apply