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PR/110338 | Senior Regulatory Affairs Specialist
| Location | India, Mumbai |
| Job Type | Permanent Full-time |
| Salary | Negotiable, based on experience |
Job Description
Position: Senior Regulatory Affairs Specialist
Designation: Mumbai
Prepare documentation and submit them to the related distributors or authorized representatives to file to the authorities. Prepare and submit documentation to respond to additional requirements by authorities. Liaison and negotiate with related distributors or authorized representatives to proceed with projects. Communicate and collaborate with Regulatory Affairs members Devise submission strategy for new products to get clearance earlier. Keep abreast of legislation, guidelines, and regulations relating to regulatory affairs for each of countries; inform and advise Japan. Ensure that products and related documents conform to the latest appropriate medical product regulations. Monitor expiration dates of licenses and apply for license renewals. Respond to audits by authorities as needed.
Notice: By submitting an application for this position, you acknowledge and consent to the disclosure of your personal information to the Privacy Policy and Terms and Conditions, for the purpose of recruitment and candidate evaluation.
Privacy Policy Link: https://www.jac-recruitment.in/privacy-policy
Terms and Conditions Link: https://www.jac-recruitment.in/terms-of-use
General Requirements
| Minimum Experience Level | Over 3 years |
| Career Level | Mid Career |
| Minimum English Level | Basic |
| Minimum Japanese Level | None |
| Minimum Education Level | Associate Degree/Diploma |
| Visa Status | No permission to work in Japan required |
Job Location
- India, Mumbai
Work Conditions
| Job Type | Permanent Full-time |
| Salary | Negotiable, based on experience |
| Industry | Medical Device |
