Cure Talent are delighted to be partnered with an established medical device company as they implement a new quality system to support their next phase of growth and operational development. As part of this transition, the business requires additional support within its Quality Assurance and Regulatory Affairs function, offering an entry point into QARA.
We have an opportunity for a Quality Assurance & Regulatory Affairs Administrator to join the team on a temporary basis, supporting the rollout of the new system and the creation and management of documentation across the business. This role is expected to run through to at least the end of 2026, with potential to extend.
As the Quality Assurance & Regulatory Affairs Administrator, you will focus on creating, formatting and structuring SOPs, templates and controlled documents from information provided by the QARA team. This is a hands-on administrative role, supporting the wider function and enabling the team to operate effectively within a structured system environment.
This is an entry level role focused on accuracy, organisation and document creation rather than ownership of QA or regulatory activities.
To be successful as the new Quality Assurance & Regulatory Affairs Administrator, you will bring strong administrative experience with excellent attention to detail and a methodical approach to document creation. You will be confident using Microsoft Office, particularly Word, and comfortable working with structured information. Experience within a regulated environment such as medical devices or pharmaceuticals would be advantageous, alongside a genuine interest in developing a career within Quality Assurance and Regulatory Affairs.
Key Responsibilities
* Create, format and maintain SOPs, templates and controlled documentation.
* Support the implementation of a new quality system through structured document management.
* Ensure documentation is clear, consistent and aligned to internal standards.
* Provide administrative support to the Quality Assurance and Regulatory Affairs function.
* Maintain documentation within the system, ensuring accuracy and organisation.
Experience and Skills Required
* Strong administrative experience with a high level of accuracy and attention to detail.
* Confident user of Microsoft Office, particularly Word for document creation and formatting.
* Experience working with structured documentation or document control is advantageous.
* Exposure to a regulated environment such as medical devices or pharmaceuticals is beneficial but not essential.
* Genuine interest in developing a career within Quality Assurance and Regulatory Affairs.
This is a practical, detail-focused role within a supportive QARA team, suited to someone who enjoys working with documentation, creating structure from information and wants exposure to a QARA environment. The position is primarily site-based in Sunbury, with flexibility to work from home one day per week.