At a Glance
- Tasks: Lead regulatory activities for medical devices and IVDs in a fast-paced environment.
- Company: TOGL(Holdings)Limited, a pioneering diagnostics company focused on gastrointestinal diseases.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to innovation in diagnostics.
- Why this job: Make a real impact in the healthcare sector by ensuring compliance and safety.
- Qualifications: Experience in regulatory affairs and knowledge of EU MDR/IVDR requirements.
The predicted salary is between 60000 - 80000 £ per year.
TOGL(Holdings)Limited, a diagnostics company focused on gastrointestinal diseases, seeks a Regulatory Manager to lead regulatory activities for medical devices, IVDs, SaMD, and genomic diagnostics in a fast-paced development environment.
You will develop and maintain Technical Documentation per EU MDR/IVDR, support regulatory submissions, and coordinate with Notified Bodies while ensuring compliance across the product lifecycle.
Regulatory Affairs Lead — Med Devices & IVDs (SaMD) in Cambridge employer: Origin Sciences
The Origin Group Limited (TOGL) is an exceptional employer, offering a dynamic work environment that fosters innovation in the medical technology sector. With a strong commitment to employee growth, TOGL provides opportunities for professional development and encourages collaboration among teams dedicated to improving patient outcomes. Located in the UK, employees benefit from a supportive culture, competitive salaries, and a generous holiday allowance, making it an ideal place for those seeking meaningful and rewarding careers in clinical research.
