Regulatory Affairs Officer/ Executive

5 days ago


Mumbai, India Rusan Pharma Full time

**Location : Kandivali WEST**

**Roles and Responsibilities**(API)
- Market : ROW- Education /Qualification : M.Sc. /B. Pharm/M. Pharm
- Experience : 2 to 6 years
- Job Profile:

- DMF filing in regulatory / non regulatory market.
- Co-ordination with site for all the data required for initial filing and queries received.
- To review the documents (Analytical, R&D, PV).
- To check suitability for filing.
- Corrections of gaps found from site
- To plan for analytical validations with QA/ ADL
- Visit the site as and when required.

**Roles and Responsibilities** (Formulation)
- Market : Africa & South Africa, South East Asia, CIS, Brazil and Mexico
- Education /Qualification : M.Sc. /B. Pharm/M. Pharm
- Experience : 1 to 3 years - Job profile:

- Role:
Regulatory Affairs Compliance
- Salary:
Not Disclosed by Recruiter
- Industry:
Pharmaceutical & Life Sciences
- Department:
Legal & Regulatory
- Role Category:
Corporate Affairs
- Employment Type:
Full Time, Permanent
- Key Skills

Regulatory Affairs

dossier

dmf

regulatory guidelines

Skills highlighted with ‘‘ are preferred keyskills
- Education
- UG:
B.Pharma in Any Specialization
- PG:
MS/M.Sc(Science) in Any Specialization,M.Pharma in Any Specialization

Company Profile
- Rusan Pharma
- Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates. The company has its own Research & Development centre at Kandivli (west), Mumbai, state of the art, Bulk Manufacturing Plant at Ankleshwar and Formulation plant at Dehradun and SEZ, Kandla having approval of MHRA (UK), MCC (SA) and other International Health Authorities. March 2008 - 82 Crs., Expected by March 2009 €“ 150 Crs.

Contact Company:
Rusan Pharma

Website:


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