Analyst- Regulatory Affairs

CK Clinical
£28000 to £30000
17 Oct 2016
16 Nov 2016
Contract Type
Oliver Care is recruiting for a Regulatory Affairs Analyst to join a global, technology-driven multi-specialty health care company at their site based in Marlow on a permanent basis.

The main purpose of the role will be:
-To provide clear, constructive regulatory advice and guidance to global project and regulatory teams.
-Ensure effective planning, tracking, archiving of activities, especially submissions, internal memos and key correspondence.
-Prepare regulatory documents for product approval in EMEA throughout the product lifecycle.

Further responsibilities will include:
-Provide regulatory support to Asia Pacific and Latin America regions with regard to Legal Manufacturer documentation.
-To support the development and implementation of processes to leverage the global infrastructure and maximise efficiency.
-Taking personal responsibility for the notification of Regulatory activities and related database entry/data accuracy for allocated projects.

In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
-Educated to degree level in a Life sciences or related field.
-Must have relevant Medical Device experience, including the registration and maintenance of products within the Europe, Africa and Middle East region.

This is an excellent opportunity to join a multi-speciality, global pharmaceutical company that delivers leading, innovative products.

CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL37347 in all correspondence.