Principle Regulatory Officer Post Approval Group

Principle Regulatory Officer

Salary: £ Competitive

Location: SouthEast London

Start: ASAP
* As a Principal Regulatory Affairs Officer, it'll be your team's job to perform the necessary regulatory tasks to help obtain the new Marketing Authorisations and maintain the existing licence portfolio as well as to support clinical trial applications for pharmaceutical products in the EU.
* Your previous experience in the pharmaceutical industry will help you compile, review and submit appropriate high quality regulatory dossiers, post-approval changes and responses to Health Authority questions in accordance with in-house standards and current legislation.
* You'll have coaching and project management skills that you'll use to ensure regulatory applications are completed to the highest standards required.
* The main responsibilities of the role are to ensure high quality data and standards are used in support of all regulatory applications to achieve rapid and successful assessment.
* You will also be required to give regulatory support to R&D pipelines, project teams, manufacturing sites, stakeholders and customers.

Must have;
* previous experience in the pharmaceutical industry
* People management skills (coaching, mentoring, leadership)
* Problem solving skills

The Regulatory team ensure that the business is compliant with the pharmaceutical legislation, the licences are granted and updated on time as required and provides the crucial link to the MHRA, which is the UK Regulatory Authority.

If you are interested in finding out more information contact or call Natalie Hopkins on 02077587311

To find out more about Real Staffing please visit www.realstaffing.com