At a Glance
- Tasks: Lead regulatory functions and shape strategic decisions for medical devices.
- Company: Join Medibeam, a forward-thinking company in the medical device sector.
- Benefits: Competitive salary, career growth, and the chance to influence global regulations.
- Other info: Onsite role in the UK with opportunities for international collaboration.
- Why this job: Make a real impact on global health by ensuring device compliance.
- Qualifications: Experience in regulatory affairs and knowledge of Class III devices required.
The predicted salary is between 60000 - 72000 £ per year.
Medibeam is seeking a Regulatory Affairs Manager to lead the day-to-day regulatory function and shape strategic decisions.
The role reports directly to the CEO and emphasizes international submissions across multiple markets.
The candidate will own technical files for Class III devices, manage complaints, liaise with notified bodies, and drive registrations globally with a focus on European market requirements.
Onsite work is required in the UK until stability is achieved.
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Global Regulatory Affairs Lead – Medical Devices (Onsite UK) employer: Medibeam
Medibeam is an excellent employer for those looking to grow within the MedTech industry, offering a supportive culture that prioritises employee development and training. With a well-established ISO 13485 quality management system, employees can expect to gain invaluable experience and skills in QA processes while enjoying the flexibility of a hybrid work model after the initial onboarding period. The company's commitment to fostering talent makes it an ideal place for individuals eager to advance their careers in a meaningful and rewarding environment.
