Job Description

● 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.

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