For all the roles (professional and lay), you must:
• be able and prepared to contribute actively to the work of the BPC;
• be able to operate effectively on a national expert scientific committee;
• be able to assimilate complex information at pace;
• be a skilled communicator
For the professional roles you must also:
• have a general understanding of the purpose and function of a pharmacopoeia and its place in the overall regulatory system (UK and Europe)
• have significant experience in the pharmaceutical industry, academia, or the hospital service, including in one or more of the following areas:
- quality control of medicinal products (human and/or veterinary), ideally with an understanding of how Quality by Design principles can be applied to the quality control of medicinal products
- analysis of biological and biotechnology products, ideally with expertise in the areas of advanced therapy medicinal products and/or biotechnologically produced proteins
- quality control of unlicensed medicines
- use and quality control of veterinary medicines
• be recognised by your peers as an eminent member of your profession, with wide and recent experience in at least one of the following areas:
- the practice of pharmacy
- analytical chemistry
- biology
- standardisation and specifications for human medicines
- standardisation and specifications for veterinary medicines
- standardisation and specifications for biological medicines
For the 2 lay member roles, you will:
• have an interest in or awareness of the issues covered by the British Pharmacopoeia Commission (BPC) from a patient or public perspective, but you will not be an expert in the areas covered within the remit of the BPC;
• have the ability to provide an independent, impartial lay contribution to the discussions, thereby giving a different view from the experts and enabling a fuller understanding of the area being discussed.