IDWG's Plastic, Reconstructive and Aesthetic Surgery EAG

1 week ago


London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

Job summary

The Interim Devices Working Group (IDWG) is looking to appoint expert members to the Plastic, Reconstructive and Aesthetic Surgery Expert Advisory Group (PRASEAG).

The PRASEAG is formed of external experts ( clinicians, scientists and lay representative/s) who provide clinical and scientific perspective on the regulation of medical devices used in Plastic Surgery, both for cosmetic and reconstructive procedures.

PRASEAG helps MHRA to better understand the risks, benefits and complications that may be caused by devices and medicines used for both reconstructive and cosmetic Plastic Surgical purposes ( BIA-ALCL).

Main duties of the job

Expertise Required:

Member of Cosmetic Practice Standards Authority (CPSA)

We are looking for aregistered Healthcare Professional who is an active member of CPSA Board.

The Member must be able to demonstrate the qualities, skills and experience to meet all the essential criteria for appointment.

Please note that only applications submitted to CSTR will be considered.

About us

The Medicines and Healthcare products Regulatory Agency (MHRA) enhances and improves 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 in this vacancy or visit:

To make an application please email your application form, CV , completed monitoring form and declaration of interest form to: CSTR, quoting the position and reference PRASEAG24-2 in the subject field.

Please note that only applications submitted to CSTR will be considered.

Person Specification

Qualifications

Essential

The members must be able to demonstrate the qualities, skills and experience to meet all the essential criteria for appointment. Be an active member of CPSA Board Must be a registered Healthcare Professional (HCP) Be an experienced practitioner who can provide the perspective of their specialism on relevant UK practice and medical device-related matters. Have the ability to represent the views of the wider CPSA and to feedback the work of PRASEAG to its members. Experience in a senior role with responsibility for making decisions related to patient safety Be experienced at assessing benefit and risk relating to patient safety and substantial and proven interest in medical devices. Ability to operate effectively on an expert scientific committee Be able to assimilate and interpret complex scientific information and formulate evidence based comments /advice at short notice Be able and prepared to contribute actively to the work of the EAG, including on issues outside of own specialism Excellent verbal and written communication skills Ability to identify solutions to difficult problems, with an objective, independent and impartial approach Flexible attitude, ability, and enthusiasm to work as a team member Be willing to develop a working knowledge and understanding of UK medical device regulatory framework and procedures Maintain strict confidentiality with respect to the work of the EAG Be able to declare conflicts of interest and adhere to the Code of Practice Be committed to the values of selflessness, integrity, objectivity, accountability, professionalism, impartiality and consistency.

Desirable

The applicant is recognised by their peers as a leader in their field Royal College, nationally recognised clinical associations, nationally recognised academic research teams The ability to network more widely is desirable. Preferably knowledgeable in the UK practice guidance issued by the CPSA with ability to influence updates to guidance.

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