Advanced treatment offerings covering commercial, quality, regulatory and operations aspects.
Develop and implement go-to-market plans for profitable product launches and work with K0Ls to pilot the product and establish a customer base.
Identifying gases and medical products scheduled to be launched in the Kingdom of Saudi Arabia, and searching for partners to successfully implement this launch.
Responsible for profitable growth as well as product operation. Responsible for registering products as medicines or medical devices.
After registration, you will manage the relevant quality and regulatory tasks (such as SFDA requirements, GMP/GDP compliance, vigilance, medical device regulation, quality management) and will be fully responsible for all regulatory obligations related to medicinal products and medical devices at SIGAS.
Represent SIGAS in authority proceedings, correspondence, inspections and audits.
Monitoring changes in the law and the companys adaptation to new legal requirements in the field of medical products and medical devices.
