The work helps ensure products meet regulatory requirements (MDR and IVDR), which is needed for CE marking and market approval.
What you will do
* Look at scientific data from studies, journals, and post-market reports
* Assess how safe and effective Abbott and competitor devices are
* Prepare clear, accurate scientific and regulatory reports
* Ensure documentation meets strict regulatory standards
* Help produce reports needed for product approvals (CE marking)
* Ensure work is high quality and delivered on time
* Collaborate with a wider scientific and clinical team
* Share findings and present information clearly
Skills and experience needed
* Degree in a scientific or technical subject
* Good scientific writing and communication skills
* Strong attention to detail
* Ability to manage changing priorities and deadlines
* Good IT skills (Microsoft Office)
Desirable
* Experience in a regulated or scientific industry (e.g., healthcare, medical devices)
* Experience with tools like Power BI or Power Automate
What they’re looking for in you
* Comfortable working in a fast-paced environment
* Able to analyse information carefully and draw conclusions
* Organised and responsible for your own work
* Keen to develop skills in scientific writing and data analysis
* A team player who can also work independently
Salary description
£22.56 - £22.56 per hour
