● Study of scientific documents.
● Collect, evaluate, organize, manage and collect information in various formats.
● Ensure compliance with regulations set by the Equipment Department.
● Up-to-date on changes in regulatory rules and regulations.
● Provide advice on company policies, practices, and systems.
● Description of requirements for labeling, storage, and packaging.
● Communication and negotiation with regulatory authorities.
● Provide advice to the company on regulatory changes.
● Write understandable brochures and information labels.
● Ensure compliance with quality standards.
● Follow up on matters related to imported shipments.
Requirements
● Bachelor's or Master's degree in Medical Engineering with relevant work experience.
● Minimum 5 years related work experience in Medical Equipment Companies.
● Experienced in the process of product registry with the Ministry of Health through imed.ir.
● Familiarity and complete mastery of ISO technical files.
● Familiarity with the range of company products.
● Familiarity with the rules of importing consumer necessities.
● Mastery of TTAC system.
● Familiarity with SOP writing.
● Familiarity with pricing.
● Familiar with the business process.
● Highly skilled in working with MS Office software and the internet.
● Highly fluent in the English Language, especially in formal correspondence and negotiation.