Regulatory Affairs Labelling Opportunity - my niche pharmaceutical client based in Berkshire is looking to appoint a talented labelling manager to be accountable for the quality and compliance of global regulations throughout the product label lifecycle.

The role incorporates involvement in the creation, review, maintenance of documentation that is associated with both marketed and investigational drug products in Europe regional area, such as EU/Local Patient Information Leaflets, SmPC, Prescribing Information, educational materials (included or not In Risk Management Plan) and some ad-hoc pieces used in market, together with primary and secondary packaging artworks.

This is a fast paced, dynamic organisation where you will have a high degree of autonomy and flexibility on a global basis and have quick access to key decision makers. In return an excellent financial package and bonus are on offer and a level of experience that is seldom found in organisations as large as this.