Description
I am currently recruiting for a Regulatory Affairs Officer based in a large Global Pharmaceutical Company for a 12 months contract based in Berkshire.
The main responsibilities of the role include all tasks associated with managing life cycle submissions with the country offices. The position is also responsible for providing submission strategy for all registration activities within the countries under responsibility. In addition you will be responsible for driving all activities required for timely and effective submission and approval of changes from the board.
The right candidate MUST have:
1. Bachelors degree or equivalent in related science or pharmaceutical field
2. Experience working in Regulatory Affairs
3. Experience of CMC to include knowledge and submissions
Desirable:
1. Negotiation with Regulatory bodies
2. EMEA regional submission requirements
This is an urgent fill so please respond with your CV immediately.