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Are you a science graduate or an industry professional looking to build a career in the high-demand medical device sector? We have an excellent opportunity for a Clinical Scientist to join a world-class clinical operations team at a major manufacturing site in Witney. In this vital role, you will be responsible for ensuring the timely delivery of high-quality technical reports in accordance with MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) guidelines. Your work will directly support CE marking, enabling the continued global supply of life-changing healthcare products. This role focuses heavily on the critical review and appraisal of clinical data, alongside the preparation of clear, accurate scientific documentation. It's a fantastic environment for someone eager to develop deep expertise in scientific writing, data evaluation, and regulatory compliance.
Job Responsibility
Gather, critically review, and assess clinical evidence from a range of sources, including scientific literature and post-market clinical follow-up data
Compile, write, and edit high-quality technical documentation and clinical evaluation reports to meet strict EU and global regulatory standards
Evaluate data for both internal medical devices and competitor products to support clinical safety arguments
Take complex data sets and present findings in an impactful, engaging, and clear way to cross-functional teams
Participate in team initiatives aimed at streamlining documentation workflows and optimizing data analysis procedures
Requirements
A higher education qualification (BSc, MSc, or equivalent) in a technical, medical, or scientific discipline
Strong communication skills with an excellent grasp of scientific/technical writing and a sharp eye for detail
The ability to adapt quickly to changing project priorities and fast-paced deadlines
Strong IT literacy, including high proficiency in Microsoft Office applications
Ideally, some prior industry-based experience working within a scientific, laboratory, or highly regulated environment (e.g., Pharmaceuticals, ISO settings, or Medical Devices)
Nice to have
Experience with data tools like Power BI or automation tools like Power Automate is highly desirable
Some prior industry-based experience working within a scientific, laboratory, or highly regulated environment