Regulatory Affairs Associate
2 weeks ago
Review regulatory guidelines for registration of Pharmaceutical Drug
- Prepare/Request/Review and compile dossier documentation as per guidelines. This includes managing BMR, MFR, PDR, AMV, and other common documents.
- Computer handling, MS Office, and other common software skills
- Rectify documentation queries from regulatory bodies
- Review artwork
- Coordinate samples and other items for submission
- 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, Fresher
Pay: ₹15,000.00 - ₹20,000.00 per month
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
Ability to commute/relocate:
- Changodar, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)
Application Question(s):
- Do you have any Pharmaceutical regulatory knowledge or background?
**Education**:
- Diploma (required)
**Experience**:
- Computer, MS Office: 1 year (required)
- Pharmaceutical or Chemical field: 1 year (preferred)
Work Location: In person
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