About the company
Our client is an established international diagnostics and life science products business with a site in Reading. Their Regulatory Affairs team is delivering a 12 month IVDR transformation project, and they need a Regulatory Affairs Assistant to support the team through it.
The role
This is a great first or second step in regulatory affairs. You will take on day to day regulatory tasks and customer regulatory queries, so the Regulatory Managers can focus on submissions. You will not write technical files or submissions yourself; you will gather, organise and prepare the information the managers need to do so.
What you will do
- Answer customer facing regulatory queries accurately and on time
- Support the day to day running of the Regulatory Affairs function
- Gather, organise and prepare documents so the Regulatory Managers can compile technical files and submissions
- Support the IVDR transformation project with tracking, records and admin
- Work closely with Quality and other teams on site
What you will bring
- Ideally 1 to 2 years in regulatory affairs, quality or a related role in IVD, medical devices or life sciences
- An interest in regulatory affairs and IVDR
- Strong organisation, accuracy and written communication
- A science degree or similar is helpful
Details
- Location: Reading, Berkshire, fully on site
- Contract: 12 month fixed term contract, full time
- Salary: £30,000 to £35,000 per year
- Start: as soon as possible
Apply below, or contact Chris Stirling, Managing Director, at chris.stirling@stirlingqr.com.
Regulatory Affairs Assistant in Reading employer: Stirling Q&R
Stirling Q&R offers a supportive environment for those looking to start or advance their careers in regulatory affairs, particularly within the diagnostics and life sciences sector. The company is currently engaged in a significant IVDR transformation project, providing employees with valuable experience and opportunities for professional growth. With a focus on collaboration and efficiency, employees can expect to work closely with experienced regulatory managers while contributing to important projects.
