Regulatory Affairs and Quality Lead

1 month ago


Crawley, West Sussex, United Kingdom Manor Royal Business District Full time

Are you a seasoned professional with a passion for regulatory affairs and quality management? We're seeking a highly skilled Regulatory Affairs and Quality Lead to join our team in the European region.

This exciting role involves overseeing and managing functions that support departmental initiatives and directives. You will be responsible for setting priorities, monitoring, and reporting on budget, planning, logistics, and acting as a regional coordinator for regulatory submissions and strategies.

As a key member of our team, you will work closely with local organizations to ensure compliance with legislation and represent our company in international regulatory bodies. Your expertise will be invaluable in supporting the development and implementation of regulatory strategies and ensuring the quality of our products.

We're looking for someone with a strong background in regulatory affairs, preferably with experience working with medical devices in the European region. Knowledge of the European Directive for Medical Devices and experience with ISO 13485 would be a significant advantage.

In return for your expertise, we offer a competitive salary, up to 25 paid vacation days, and a range of benefits including private medical insurance, a hybrid work option, and a cycle to work scheme.

So if you're a motivated and experienced professional looking for a new challenge, please get in touch to learn more about this exciting opportunity.



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