Posted on Jan 19, 2019 by Anonymous
The main focus of the role is to be responsible for representing the RA/QA function for all Field Safety Corrective Actions (FSCA), including reporting related activities to the Competent Authorities. Assist the Group Manager with other RA duties as required. Dealing with product registrations. Managing Certificates of Free Sale (CFS) with the MHRA.
The successful candidate will have had already a sound career in this area and will have :-
Minimum 1-2 years experience in Regulatory Affairs, or a minimum 3 years Quality Assurance activities related to medical devices or pharmaceuticals or a minimum 2 years legal environment experience.
• Excellent English, both written and verbal.
• Proficient in Word and Excel.
Experience in MS Access, MS Visio, Agile, and SAP desirable. Proficient in Word and Excel, and good writing skill is needed. Experience in MS Access, MS Visio, Agile, and SAP desirable.
Send cv on a Word document please