Job Position :- Regulatory Associate/ Specialist
Job Description:- The Regulatory Associate/ Specialist -Global Labelling-DRA (INDIA)is responsible for activities of DRA-Global labelling for Novartis Pharma products, which include & are not limited to Support Global Labelling Managers at Basel from India for providing the DRA-GL regulatory inputs (e.g. PSUR, PSB, BSS, PIL, CDS etc.). The activities also include supports the GL planning and the monitoring of the worldwide implementation of corporate agreed product information changes (Core Data Sheet (CDS) updates and amendments) for international Novartis Pharma products in order to achieve international harmonization of Pharmaceutical Product Information.
Job Description:- The Regulatory Associate/ Specialist -Global Labelling-DRA (INDIA)is responsible for activities of DRA-Global labelling for Novartis Pharma products, which include & are not limited to Support Global Labelling Managers at Basel from India for providing the DRA-GL regulatory inputs (e.g. PSUR, PSB, BSS, PIL, CDS etc.). The activities also include supports the GL planning and the monitoring of the worldwide implementation of corporate agreed product information changes (Core Data Sheet (CDS) updates and amendments) for international Novartis Pharma products in order to achieve international harmonization of Pharmaceutical Product Information.
Desired Profile :- Masters/ Bachelors degree in Pharmacy/ Medicine (e.g. Pharmacy, Biotechnology, Pharmacology, Quality Assurance) or equivalent. Excellent English required (oral and written).
1 - 8 years practical experience (Medical affairs, Regulatory, Clinical or Quality Assurance)
Contact :-
Contact :-
Meghna
Novartis Healthcare Pvt Ltd
iLabs Centre,
No. 18, Software Units Layout
Madhapur Hyderabad,
Andhra Pradesh,INDIA 500081
040-66576598
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