Analyst for Regulatory Affairs department at Novo Nordisk | M.Pharm, B.Pharm, M.Sc

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

Post : Analyst for Regulatory Affairs department

About the department
Global Regulatory Affairs (GRA) in Bangalore consists of eight departments that work across our global processes and support both colleagues in Head Quarter Denmark (DK) as well as colleagues in our affiliates all over the world. As the area is growing, the total area will by midyear 2019 consist of approximately 120 dedicated employees. Regulatory Operations, Global Service Centre (GSC) is an integral part of Regulatory Operations DK. The objective of this team is to ensure efficient and competitive Regulatory Operations to support Regulatory Affairs HQ and RA Affiliates. The team provides the services in Submission Management, Regulatory Information Management and Operational Graphic Design.

The position
As Regulatory Affairs (RA) Analyst, you will be responsible for Register Data management handling and addressing the queries of stakeholders. You would also be responsible for data entry tasks such as data entry in Regulatory database (RIMS) for Registrations, Regulatory changes and updates, supporting and ensuring RIMS support tasks.

Candidate Profile
• Graduate / Post Graduate or comparable degree in Science/ Pharmacy/ Computer related field
• 6-8 Years
• Knowledge in Data Entry & Data Management
• Knowledge in Regulatory Affairs
• Knowledge in Register Database preferred
• Knowledge in MS-Office
• Take initiative, systematic and organised, thorough and analytical, service minded and customer oriented
• Good communication and English proficiency
• Stakeholder Management

Additional Information
Qualification : M.Pharm, M.Sc, B.Pharm
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th January, 2020