Regulatory Affairs Executive

3 months ago


Mumbai, India approach Full time

complete, accurate and comply with applicable regulatory requirements, leading to timely approval of new product

registration in India.
- Notify and update CDSCO of any changes of particulars / documents related to product registration if necessary.
- Ensure timely submission of changes to approved products when required.
- Watch notifications of CDSCO and other relevant organizations to collect latest regulations related to medical device.
- Maintain registry of product registration record and database.
- Communicate with Manufacturer who supplies medical devices

Education & Experience:

- Diploma in Medical Sciences or equivalent
- At least 2 years of relevant experience in regulatory affairs in the medical device / healthcare industry
- Knowledge of Drugs and Cosmetics Act and medical device regulations in India.

**Salary**: ₹198,172.73 - ₹776,281.41 per year

**Benefits**:

- Provident Fund

Schedule:

- Day shift

Supplemental pay types:

- Performance bonus

Ability to commute/relocate:

- Mumbai Suburban, Maharashtra: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 4 years (required)

**Speak with the employer**
+91 8108726392



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