Regulatory Expert

Avin Darou Tehran

Posted 5 years ago

Job

Company

Salary

Applicant Insights

Job Description

• Registration of new products
• GMP and GDP audit of distribution companies
• Following up of variations of registered products
• Supervision of quality processes
• Gathering Pharmacovigilance and ADR reports
• Develop professional relationships with MOH staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations
• Develop professional relationship & collaboration with distributers and wholesalers
• Preparation of forms to add new molecule to IDL
• Preparation of related SOP’s for regulatory process
• Ensure quality compliance in shipment of products
• Train employees in quality processes and managing quality procedures

Requirements

• University Qualifications: Pharmacist, Master in Biomedical engineering, Chemistry, Hematology, Microbiology, Medical Engineering or related medical majors. • Fluency in writing, reading and speaking of English language • Preferable age between 25-32 years • Ability to work in a team • Good command of computer knowledge (MS. Office) • Ability to travel within the country and abroad • Previous experience in regulatory of medical device is a plus point

Employment Type