About this role
Job summary
Please note that applications submitted to [email protected] will be considered only.
The Medicines and Healthcare Products Regulation Agency (MHRA) is seeking to appoint an expert in Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) requirements in relation to proposed regulatory action against a manufacturing or wholesale licence which has been referred to the Review Panel.
The purpose of the Review Panel is to hear oral representations, in accordance with the legislation, from licence holders who disagree with a proposed decision made by the MHRA. The Review Panel members are greatly appreciated for making their professional expertise available for a public service role that carries out statutory and non-statutory reviews of proposals, decisions and provisional decisions taken by Medicines and Healthcare Products Regulatory Agency.
Main duties of the job
Expertise Required: Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) requirements in relation to a manufacturing or wholesaling of medicinal products.
To be considered, you must be able to demonstrate that you have the qualities, skills and experience to meet all the essential criteria for appointment.
About us
The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.
Job description Job responsibilities
For full details on job description, please refer to advert attached and visit:The Review Panel (MHRA) - GOV.UK
To make an application please email your application form, CV, completed monitoring form and declaration of interest form to: [email protected], quoting the position and reference RP26-4 in the subject field.
Please note that applications submitted to [email protected] will be considered only.
Person Specification
Experience Essential
To be considered, you must be able to demonstrate that you have the qualities, skills and experience to meet all the essential criteria for appointment. Be recognised by their peers as a leader in their field. They should have extensive and recent experience in the specified areas. Have or demonstrate ability to operate effectively on a national expert panel Be a skilled communicator Be able to assimilate complex scientific information at short notice and apply this to their expertise in consumer affairs Be able and prepared to contribute actively to the work of the Review Panel
Desirable
Have an understanding of medicines regulation and be willing to develop this further
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details Employer name Medicines and Healthcare Products Regulatory Agency
Address Medicine & Healthcare Regulatory Agency
10 South Colonnade
London
E14 4PU
United Kingdom
Employer's website https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency (Opens in a new tab)