Regulatory Affairs Officer
2 months ago
Review regulatory guidelines for registration of Pharmaceutical Drug and/or Medical Device for the market especially Central & South America, CIS, Asia-Pacific, etc
- Request, Review and compile dossier documentation as per guidelines
- Rectify documentation queries from regulatory bodies
- Coordinate with team members to ensure swift workflow
- Prompt response, attention to detail, good communication skills
- Ability to work at fast pace
- Other duties as assigned
**Job Types**: Full-time, Permanent
Pay: ₹15,000.00 - ₹50,000.00 per month
Supplemental Pay:
- Yearly bonus
Ability to commute/relocate:
- Surat, Gujarat: Reliably commute or planning to relocate before starting work (preferred)
**Education**:
- Diploma (preferred)
**Experience**:
- Document preparation for Central & South America market: 1 year (required)
Work Location: In person
Application Deadline: 14/09/2024
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