Job Description
- Study scientific documents.
- 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.
- Communicate and negotiate 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.
- Experience in the process of product registry with the Ministry of Health through imed.ir.
- Familiarity with ISO technical files.
- Familiarity with the range of company products.
- Familiarity with the rules of importing consumer necessities.
- Mastery of the TTAC system.
- Familiarity with SOP writing.
- Familiarity with pricing.
- Familiar with the business process.
- At least 5 years of related work experience.
- Highly skilled in working with MS Office and the Internet.
- Fluent in English, especially in formal correspondence and negotiation.
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