IDWG's In Vitro Diagnostics Expert Advisory Group
The closing date is 28 November 2025
Job summary
IMPORTANT: Application Instructions
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To apply for this position, please email your application form, completed declaration of interests form and monitoring form directly to CSTRecruitment@mhra.gov.uk. Only applications received via this dedicated mailbox will be reviewed.
The Interim Devices Working Group (IDWG) is looking to appoint professional members to the In Vitro Diagnostics Expert Advisory Group (IVD EAG).
The IVD EAG is a subgroup of the IDWG that provides independent expert advice to the Medicines and Healthcare products Regulatory Agency (MHRA) on the development, implementation, and evaluation of IVD devices. The groups objective is to ensure that IVD regulations, guidance and regulatory practices support innovation, maintain high standards of safety and efficacy, and align with international and domestic leading practices.
IVD EAG is formed of experts in the field of in vitro diagnostics, including scientists, engineers, clinicians, pathologists, and diagnostics regulatory specialists. Representatives from relevant government departments and agencies, e.g. NICE, Devolved Administrations, NIHR, UK HSA, etc. Non-industry stakeholders, including representatives from academia and learned organisations such as the Royal Colleges and Biomedical faculties and patient or patient group representatives.
Main duties of the job
As a member you will:
Take full account of the evidence in making decisions and consider the analysis and interpretation of the evidence prepared by MHRA.
Consider equality, diversity and inclusion in all of the EAG discussions.
Have a flexible attitude, ability and enthusiasm to work as a team member.
Assessing benefit and risk in relation to evidence presented in order to contribute expertise to generate effective actions to mitigate risk.
Read papers in advance of meetings.
Occasionally comment on documents in between meetings by email.
Keep the work of the EAG confidential Declare conflicts of interest and adhere to the Code of Practice (link).
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.
Details
Date posted
13 October 2025
Pay scheme
Other
Salary
Depending on experience £0
Contract
Fixed term
Duration
3 years
Working pattern
Part-time, Flexible working, Home or remote working
Reference number
K0015-IVDEAG25-2
Job locations
Medicine & Healthcare Regulatory Agency
10 South Colonnade
London
E14 4PU
Employer details
Employer name
Medicines and Healthcare Products Regulatory Agency
Address
Medicine & Healthcare Regulatory Agency
10 South Colonnade
London
E14 4PU
Employer's website
Employer contact details
For questions about the job, contact:
Committee Services - Recruitment Team
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