Regulatory Affairs Associate

5 days ago

Chandigarh Chandigarh, India Sysmed Medical Technologies Full time

**Documentation Executive for Regulatory Compliance**

1) Ensure compliance with regulatory requirements for product registration, renewals, and variations.

2) Prepare and review technical documents, including stability data, product formulation, and analytical reports.

3) Liaise with internal departments such as R&D, Quality Assurance, Quality Control, and Production to collect required documents.

4) Communicate with regulatory authorities and clients to address queries and ensure smooth approval processes.

5) Monitor and update changes in regulatory guidelines.

6) Implement necessary updates in documentation and processes to align with regulatory changes

**Preferred Experience**: Minimum 1 years of experience in Regulatory Affairs

Prior experience in medical equipment will be an added advantage

Detail-oriented with strong documentation and organizational abilities.

Proficiency in MS Office (Word, Excel, PowerPoint).

Contact Person: - Esha Fotedar

9056699984

**Job Types**: Full-time, Permanent

Pay: Up to ₹25,000.00 per month

**Benefits**:

- Health insurance
- Paid time off

Schedule:

- Day shift

Work Location: In person

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