Qualified Person and Regulatory Affairs Manager
Moad has vast experience and unique expertise in nuclear pharmacology and regulatory affairs.
Since joining the company in 2010, he has led several key roles in radiopharmaceutical synthesis, development, quality assurance and quality control.
During the past years Moad has been diligently working in the sterile production site, providing regulatory and technical expertise to cross-functional teams while facilitating audits by local and global regulatory authorities.
Moad is highly involved, regulatory-wise, in the development of new products and renowned for his contribution to defining target product profiles that may be compliant with regulatory requirements.
He is highly meticulous and pays great attention to details, even the smallest ones.
In his free time, Moad aspires to persist in sports, especially bike riding.
Moad holds a BSc in Pharmacy from the Hebrew University and a Master’s Degree in Pharmacology from the Tel Aviv University. He also holds a Nuclear Pharmacy Certification by the Purdue University (USA) along with a Quality and Organizational Excellence Certification.