Position Objective:
Regulatory Affairs Officer acts as a link between Company and the regulatory authorities, ensuring that the products that are distributed by Maquet Middle East are in compliance with the appropriate legislation.
Essential Duties and Responsibilities:
- Manage and facilitate all medical devices related registration activities for Middle East and Africa Region.
- Complete forms and requests originating from government agencies.
- Maintain contact with regulatory authorities and company headquarters in Germany.
- Provide the Project teams and Managers with regulatory input in order to obtain timely regulatory approvals for the products (medical devices) as part of the product development planning.
- Assure compliance with Export regulation for US manufactured products (OFAC & BIS).
- Update licensing and collect information on registration instructions and regulations.
Job Details
| Date Posted: | 2015-01-25 |
| Job Location: | Dubai, United Arab Emirates |
| Job Role: | Law/Legal |
| Company Industry: | Medical/Hospital; Healthcare, Practitioner and Technician; Biotechnology |
| Monthly Salary: | US $3,000 |
Preferred Candidate
| Career Level: | Entry Level |
| Degree: | Bachelor's degree / higher diploma |
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Company:
Date Posted: January 25, 2015 at 02:40PM
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Regulatory Affairs Officer (Arabic Speaking) - Maquet Middle East
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