Regulatory Affairs Specialist for Medical Devices
We are seeking a highly skilled Regulatory Affairs Specialist to join our team in Galway, Ireland. As part of our medical device start-up, you will be responsible for supporting regulatory activities and ensuring compliance with health regulations.
The ideal candidate will have at least 7 years of relevant experience in the medical device sector and possess strong communication and analytical skills. You will also develop submissions for product approvals and work closely with cross-functional teams to drive business growth.
This is an exciting opportunity for professionals who want to make a meaningful contribution to the development of innovative medical devices while working in a dynamic environment.
To succeed in this role, you should have:
* A degree in Life Sciences or related field
* At least 7 years of experience in Regulatory Affairs within the medical device industry
* Proven track record of developing successful regulatory strategies and managing complex projects
Benefits:
* Mentorship from experienced professionals in your field
* Ongoing training opportunities
The job involves supervising other employees.