Zimmer Biomet in Swindon is seeking an experienced regulatory writer to develop and maintain clinical evaluation plans, reports and post-market documentation for medical devices. You will analyze NJR data, appraisal strategies, and ensure traceability across regulatory requirements while collaborating with regulatory, clinical and development teams.
The role requires rigorous scientific writing, attention to detail, and the ability to manage multiple deliverables and deadlines.
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Clinical Regulatory Medical Writer (CERs, PMS, PMCF) in Swindon employer: Zimmer Biomet
Zimmer Biomet is an exceptional employer, offering a dynamic work culture that prioritises collaboration and innovation in the healthcare sector. Employees benefit from comprehensive training programmes and opportunities for professional growth, all while making a meaningful impact on patient care through their work with orthopaedic surgeons and theatre staff. Located in the United Kingdom, the company fosters strong relationships within the medical community, ensuring that team members are integral to advancing healthcare solutions.
