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Scientific and Procedure Advisor

3 months ago

London, Greater London, United Kingdom Medicines and Healthcare products Regulatory Agency Full time

We are currently looking for a
Scientific and Procedure Advisor to join our
Authorisation Lifecycle Function within the
Health Quality and Access group.

This is a
full-time opportunity, on a
permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU. Please be aware that this role can only be worked in the UK and not overseas.

We are currently implementing a flexible, hybrid way of working, with a minimum of 4 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business.

Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 8 days a month, with the remainder of time worked either remotely or in the office.

Some roles will need to be on site more regularly. Remote working is potentially available for some specific roles. Please discuss this with the recruiting manager before accepting an appointment.

Who are we?


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.


The objective of the Healthcare Quality and Access portfolio is to drive quality and critically appraise benefits and risks to inform robust decisions on healthcare access including accelerated access pathways.

It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable authorisation and market access, as well as ensuring compliance with regulations and standards.

The Authorisation Lifecycle function is an enabler, central to delivery of the frontline HQA group. It includes data assurance and quality, high-volume certification work and coordination and support to the frontline functions.

It also includes some more complex activity that supports across the product lifecycle such as medicines and medical devices, borderline, patient information and medicines advertising.


What's the role?

Key responsibilities:

  • Assessment of variations subsequent to the grant of a marketing authorisation.
  • Work collaboratively to drive continuous improvement within the group.

Who are we looking for?

  • A degree in chemistry, pharmacology or other scientific discipline, or relevant experience.
  • An ability to communicate effectively with internal and external stakeholders, with a proven ability to clearly explain information verbally and by written communication.
  • Good personal work organisation, attention to detail and analytical or assessment skills, including the ability to make sound decisions while working to tight deadlines.
  • A proactive approach to problem solving in a multidisciplinary, targetorientated team.
If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification

The selection process:

-
Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.


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 statement of suitability provided. You can view the criteria for this role in the job description.

Closing date: 30 August 2023

Interview Dates: 11/12/13 September 2023

Any move to the MHRA from another employer will mean you can no longer access childcare vouchers. This includes moves between government departments. You may however be eligible for other government schemes, including Tax-Free Childcare. Determine your eligibility here.

If you are not satisfied with the response you receive, you can contact the Civil Service Commission at:

Civil Service Commission

Room G/8

1 Horse Guards Road

London

SW1A 2HQ