At a Glance
- Tasks: Lead regulatory strategy for medical devices and diagnostics in the EU and UK.
- Company: Join TOGL(Holdings)Limited, a pioneering diagnostics company.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Be part of a dynamic team driving advancements in gastrointestinal diagnostics.
- Why this job: Make a real difference in healthcare by shaping regulatory pathways for innovative products.
- Qualifications: Experience in regulatory affairs for medical devices and strong collaboration skills.
The predicted salary is between 63000 - 77000 £ per year.
TOGL(Holdings)Limited, a diagnostics company focused on gastrointestinal diseases, seeks a Regulatory Manager to lead development through EU MDR/IVDR and UK regulatory pathways for medical devices, IVDs, Sa MD and genomic diagnostics.
You will shape regulatory strategy, prepare technical files, supervise PMS, and collaborate with R&D, software, QA and clinical teams to integrate regulatory requirements across the product lifecycle.
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Regulatory Affairs Leader – Medical Devices & IVDs (EU/UK) 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.
