DRA Associate

Job description

Job Description

A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. Novartis and its associated companies are always looking for talented employees globally. We are engaged in advance preparation for potential position openings. Submit your CV/resume now to join our talent pool for the position described below. Please note that you are not applying for a current vacancy, but are submitting your CV/resume for consideration for future, possible opportunities. We look forward to receiving your information.

Job Purpose - the registration of new drug products, the maintenance of registration of approved drug products and the maintenance of DRA compliance KPIs as per NVS guidance in order to ensure viability of these products in the marketplace. This will include
- New Product Registrations
- Maintenance of registered products
- Manage health authority queries for variations & renewals
- Manage new or renewal registration of manufacturing sites
- Update local archives for manufacturing site new/renewal, variation update, renewal update
- Develop and maintain product information (with supervision)
- Assist Medical Information and Quality Assurance
- Maintain internal database
Novartis is an Equal Opportunity Employer.

Desired profile

• Tertiary qualified – Pharmacy or Science (majoring in a life science or chemistry) with or without postgraduate qualifications
• Languages: Arabic and English written and spoken are mandatory
•1-3 years experience as an associate in regulatory affairs dealing with a wide variety of registration projects and issues