Officer/ Executive- Regulatory Affairs- Pharma

1 month ago


Mumbai, India HRD House Full time

From 3 to 6 year(s) of experience- ₹ 3-7 Lacs P.A.- Mumbai (All Areas)**Job description**

**You will be responsible for,**

Preparation for registration/renewal of registration, manufacturing license with products, WHO
- GMP Certificate, MSO registration, etc.

Certificates, export NOCs from CDSCO, COPPs, plan approvals, technical staff registration and

Approval, public testing labs approval, etc.

ROW Market.

2. Preparation & review of product registration/renewal of dossiers (CTC/ACTD) for Asian & African countries (ROW).

3. To ensure regulatory compliance as per D&C Act and Marketing authorizations.

4. To check the artworks for compliance with regulatory and pharmacopoeia requirements of

Products.

5. To ensure regulatory compliance as per D&C Act and Marketing authorizations.

Key Skills
regulatory affairs
AsiaAfricaRA
Skills highlighted with ‘‘ are preferred keyskillsEducation
- UG:_B.Pharma in Any Specialization
- PG:_MS/M.Sc(Science) in Any Specialization,M.Pharma in Any Specialization

**Company Profile**:
HRD House

Reputed Pharma Company.

**Thanks & Regards,**

**Sakshi Raotole**

**HRD House - Mumbai**

**(Div Pharma Talent Search)**

**Mulund (East), Mumbai-400081.**

**Salary**:
3-7 Lacs P.A.

Industry:
Pharmaceutical & Life Sciences

Department:
Legal & Regulatory

Role Category:
Legal & Regulatory - Other

Role:
Legal & Regulatory - Other

Employment Type:
Full Time, Permanent



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