Regulatory Affairs Specialist–Medical Devices & Supplements

SGS in Dubai is seeking a Regulatory Affairs Specialist to manage end-to-end regulatory submissions across the Middle East, including the UAE and GCC markets. You will prepare and review regulatory dossiers, ensure compliance with EU MDR requirements, and liaise with internal teams and regulatory authorities.

This full-time role demands at least 5 years in regulatory affairs, dealing with medical devices and supplements. Ideal candidates will hold a relevant bachelor's degree and have strong documentation and stakeholder management skills.