Requirements

• Review, compile and keep up to date technical files for medical devices and cosmetic products.
• Monitor European and local regulations and legislation related to medical devices and cosmetics.
• Ensure product compliance with applicable requirements.
• Manage EUDAMED, GREMDIS, and CPNP databases.
• Communicate with relevant authorities and notified bodies.
• Advise other departments on regulatory and compliance matters.

Qualifications

• BSc in Life Sciences (Pharmacy, Chemistry, Biology, relevant field).
• 3+ years of hands-on experience in Regulatory Affairs within the Medical Device and Cosmetics industry
• In depth understanding of medical devices regulations, cosmetics regulations and ISO 13485:2016
• Fluent written and spoken English
• Excellent MS Office skills
• Strong organization skills, multi-tasking and able to meet deadlines
• Excellent communication skills and collaborative mindset

We offer

• Competitive salary.
• Private medical insurance scheme.
• Continuous Education.
• Ability for a successful career in the fast-growing health sub-sector.

All CVs will be treated with strict confidentiality.