Global IVD Regulatory Affairs Specialist

ARC Regulatory, based in Belfast, seeks a professional to enhance their project teams by providing regulatory compliance solutions. This role involves researching regulatory submission documents, managing IVD study requirements, and contributing to regulatory guidance documents. Candidates should possess an engineering or scientific degree with over 5 years of experience in GMP/GLP environments, alongside excellent communication and analytical skills. Join the team to support access to life-saving therapies through compliance excellence.#J-18808-Ljbffr…