Pharmaceutical Assessor Unlicensed Medicines - £60,778 - £68,422 p.a. + benefits

Medicines and Healthcare products Regulatory Agency

26d ago

Applications are closed

Job
Full-time
Mid & Senior Level
Government & Politics
Healthcare
London

Requirements

Have experience in quality assurance, manufacturing/assembly of medicines and its implications on clinical outcomes and evaluation of risk to patients.
Have worked in Pharmaceutical Industry, NHS quality assurance or manufacturing roles, or relevant roles within a competent authority, and a thorough working knowledge of Good Manufacturing and Distribution Practices, regulations underpinning pharmaceutical manufacture and their implications on the safe use of medicines.
Be able to demonstrate experience of developing successful relationships with both internal and external stakeholders, with excellent communication skills.
Hold a degree in a relevant science (e.g. pharmacy, medicine).
Knowledge in one or more relevant scientific areas or broader knowledge across the range of scientific activities in relation to the pharmaceutical development, manufacture and quality assurance of human medicinal products.

Responsibilities

Assess notifications for importation into the UK of unlicensed medicinal products received under SI 2005/2789 regulation 167 and Schedule 4 against known patient safety or product quality issues affecting unlicensed medicines, to determine if a non‑objection or objection to import should be issued. Decisions must be made in a timeframe appropriate to the urgency of the issue, and on the information available at that time.
Promptly update agency, group or team and work management databases to reflect the progress of own work.
Display a high level of attention to detail to ensure up to date accurate data and documents are held on internal databases and relevant archives.
Use own and agency resources in line with agency and group strategy to meet targets.
Work with Department of Health & Social Care Medicine Supply Team, the NHS Medicines Value and Access Directorate and the NHS Specialist Pharmacy Service to highlight and manage supply disruptions.
Work in conjunction with Importers, Manufacturers and Marketing Authorisation Holders to gather sufficient information to make informed decisions regarding supply of unlicensed medicines and to agree proposed courses of action.
Provide regulatory and scientific advice, and guidance to external stakeholders to facilitate and enable continuity of supply of medicinal products in the UK.
Provide regulatory and scientific advice to MHRA colleagues across the agency.
Work with Communications and Engagement and Partnerships groups to ensure media handling and press lines are accurate, effective and commensurate to the risk.
Develop good working relationships and communicate effectively with colleagues and other internal and external stakeholders.
Provide support to other activities affecting medicine supply such as public health emergencies, ensuring flexibility and engagement with internal and external stakeholders.
On call duty rota commitment.

FAQs

What is the location of the Pharmaceutical Assessor position?

The position is based at 10 South Colonnade, Canary Wharf, London, E14 4PU.

What is the salary range for the Pharmaceutical Assessor role?

The salary range is £60,778 - £68,422 per annum, plus benefits.

How many days are required to work on-site per month?

A minimum of 8 days per month is required to work on-site, with the possibility of increasing to 12 days depending on business needs.

What qualifications are required for this position?

Candidates must hold a degree in a relevant science, such as pharmacy or medicine.

Is prior experience in the pharmaceutical industry necessary?

Yes, experience in the Pharmaceutical Industry, NHS quality assurance, or manufacturing roles is required, along with a thorough knowledge of Good Manufacturing and Distribution Practices.

What are the primary responsibilities of the Pharmaceutical Assessor?

Responsibilities include assessing notifications for the importation of unlicensed medicines, providing regulatory advice, and supporting inspectors and licensing colleagues.

Are there opportunities for professional development in this role?

Yes, ongoing learning and development opportunities are provided.

What is the closing date for applications for this role?

The closing date for applications is 10th April 2026.

Will successful candidates undergo background checks?

Yes, successful candidates must pass a criminal record check and other security checks.

Is this position eligible for the Civil Service Pension Scheme?

Yes, the role includes eligibility for the Civil Service Defined Benefit Pension scheme.

Will I need to provide evidence of my qualifications during the application process?

Yes, applicants will need to provide proof of qualifications and experience as part of the application process.

Medicines and Healthcare products Regulatory Agency

Protecting and improving public health and supporting innovation through scientific research and development.

Government

Industry

1001-5000

Employees

2003

Founded Year

Mission & Purpose

The Medicines and Healthcare products Regulatory Agency, an executive agency of the Department of Health and Social Care, exists to 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. We deliver this through three distinct yet complimentary business centres: the MHRA regulatory centre, the National Institute for Biological Standards and Control (NIBSC) and the Clinical Practice Research Datalink (CPRD). With a range of interesting specialist opportunities on offer, with plenty of scope to develop your career within a leading and multifaceted scientific organisation, why not consider a career with us at our offices in central London or Hertfordshire.