Regulatory Governance Expert at Medicines and Healthcare products Regulatory Agency
London, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

04 Sep, 25

Salary

0.0

Posted On

24 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

We are currently looking for a Regulatory Governance Expert to join our Innovation and Compliance Function within the Healthcare Quality and Access Group.

PROVISION OF GUIDANCE

Detailed understanding of relevant aspects of the human medicine’s regulations (particularly in regard to unlicenced medicines and the manufacture and wholesale distribution) and the Blood safety and quality regulations.
If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification!
Please note: The job description may not open in some internet browsers. Please use Chrome or Microsoft Edge. If you have any issue viewing the job description, please contact careers@mhra.gov.uk

THE SELECTION PROCESS:

We use the Civil Service Success Profiles to assess our candidates, find out more here .

  • Online application form, including questions based on the Behaviour, Experience and Technical Success Profiles. Please ensure all application questions are completed in full; your application may not be considered if any responses are left blank. Our applications are CV blind, and our Hiring Managers will not be able to access your CV when reviewing your application.
  • Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.

In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of candidates having a d etailed understanding of relevant aspects of the human medicine’s regulations (particularly in regard to unlicenced medicines and the manufacture and wholesale distribution) and the Blood safety and quality regulations.
Applicants are assessed on whether they meet any mandatory requirements as well as the necessary skills and experience for the role. Applications are scored based on the competency-based answers provided- ensure you have read these thoroughly and allow sufficient time. You can view the competencies for this role in the job description.

Responsibilities

WHAT’S THE ROLE?

Provide lead advisory and guidance for senior managers and external enquirers in relation to compliance with the blood safety and quality regulations, unlicenced medicines and the manufacture and wholesale distribution of human medicines, including Advanced Therapy Medicinal Products (ATMPs), investigational medicinal products (IMPs) brokering of medicines, the manufacture, importation and distribution of active substances.

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