Job Reference: 22290
Job Duration: 6 months
Start date: ASAP
Description:
* Responsible for supporting activities that initiate and maintain international product approvals for Wave 2b and 3 countries.
* Partnering closely withother members of the Strategy Implementation Group, Dossier Excellence, Regional Portfolio Leads and Regulatory Operations teams.
* Provides support for Wave 2b and 3 market registrations and license renewals.
* Providing documentation to support international registration and tender requests.
* Prepares responses to questions and requests from health authorities for product registrations.
* Managing a significant amount of proprietary information in a confidential manner to prevent loss ofintellectual property.
* Ensures compliance with regulatory agency regulations and interpretations
* Provides solutionsto a variety of problems of moderate scope of complexity.
* Maintains and archives all regulatory documentation.
- Theideal candidate will have over 2 years experience within regulatory Affairs.
- Knowledge of all regulatory documentation
-Knowledge of MRP, DCP and national procedure.
Industry: Pharmaceuticals
Salary: £18.00 - £21.00 per hour
Salary Benefits:
Vacancy Type: Contract
Job Skills: pharmaceuticals, regulatory affairs, CMC, publishing, Authoring, MRP, DCP, dossier, regulations
Contact Name: Eddie Cooper
Website: -
Direct Application URL: -