Regulatory Affairs Associate

2 weeks ago


Changodar Ahmedabad Gujarat, India Swiftmed International Private Limited Full time

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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