Skip to main content

Opening in Naprod Lifesciences for Drug Regulatory Affair Executive for Pharma R&D

 

Clinical courses

Naprod’s vision is to become a world class player in oncology through excellence in innovation, discovery of new manufacturing processes / drug delivery mechanisms and consistently high quality of production. We commenced operations in 1994 with the inauguration of our ultra-modern facility for the production of generics and formulations for oncology and other therapeutic applications. We are one of the pioneers in India in lyophilization.
We identified, very early, the need for achieving self - sufficiency in formulations as well as in Active Pharmaceutical Ingredients (APIs) , and our achievements reflect this focus. We launched our (APIs) in year 1994 & now have to our credit a number of new manufacturing processes & drug delivery mechanisms.

Posts: REGULATORY AFFAIRS Executive

Job Description:
1.  DOSSIER PREPARATION CTD AND ACTD FOR REGULATED MARKET.
2.  PREPARATION OF DOSSIER FOR REGULATED MARKET.

Candidate Profile:
SUCCESSFUL CANDIDATE IN M.PHARM WITH MINIMUM 2 YEARS EXPERIENCE IN CTD DOSSIER PREPARATION CAN APPLY.
SHOULD BE AWARE OF ANVISA, TGA AND MSS GUIDELINES.
PHARMA FILED EXPERIENCE SHOULD BE AN  ADDED ADVANTAGE.
 CANDIDATE WHO WILLING TRAVELL IN MIRA ROAD AREA ONLY NEED TO APPLY.


Additional Information:
Experience: 2-4 years
Location:
Mumbai
Education: B.Pharm, M.pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area:
DRA
Compensation: Rupees 1,75,000 - 2,00,000

Apply/Send resume at, ranjith.kaithakkal@naprodgroup.com


See All   Naprod Jobs   B.Pharm Alerts   B.Sc Alerts   M.Pharm Alerts   M.Sc Alerts

See All   Other Jobs in our Database

PharmaTutor Placements