Quality Lead

Quality Lead

Full-Time 40000 - 50000 £ / year (est.) No working from home possible
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Lead quality assurance efforts in a dynamic health and safety environment.
  • Company: Join the Medicines and Healthcare products Regulatory Agency, enhancing public health daily.
  • Benefits: Enjoy a competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Be part of a supportive team with excellent career advancement opportunities.
  • Why this job: Make a real difference in healthcare by ensuring quality standards are met.
  • Qualifications: BSc in a biological discipline and experience with ISO 17025 Quality Management Systems.

The predicted salary is between 40000 - 50000 £ per year.

We are currently looking for a Quality Lead to join our Health & Safety and Quality Assurance Function within the Science and Research group. This is a full-time opportunity, on a permanent basis. The role will be based in South Mimms, Hertfordshire.

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 Quality Assurance Team in the HSQA Function is responsible for maintaining the ISO 17025, ISO 9001 and HTA Quality Management Systems at the MHRA South Mimms campus providing guidance and support to management and scientists to ensure compliance to all relevant Standards, Directives, Regulations and Guidelines.

What’s the role?

The successful applicant will be expected to provide advice, support, guidance and training to Scientists with respect to Quality Management Systems (QMS) to support Control Testing and Batch Release testing of biological medicines work and in particular ISO 17025, WHO and EDQM requirements.

Key responsibilities:

  • Day to day management of the Control Testing Quality Management System (QMS) in line with the relevant Standards and Agency’s needs and providing advice, support, guidance, direction, training, trouble shooting and problem solving as required.
  • Carry out audits to support the Agency’s Quality Management Systems (QMS) and review audit findings to ensure that they add value and continually improve the QMS.
  • Ensure that the Agency’s Control Testing activities comply with the requirements of ISO 17025, WHO and EDQM Quality Management Guidelines and when necessary review, develop and implement harmonised QA practices in the Operational Functions with respect to ISO 17025, WHO and EDQM Requirements.
  • Develop, co-ordinate and deliver the ISO 17025 QMS training programme to support the QMS and ensure that staff at the South Mimms campus understand their responsibilities when carrying out Control Testing activities.

Who are we looking for?

Our successful candidate will:

  • BSc in a relevant biological discipline e.g. biochemistry, microbiology, immunology, molecular biology and experience of detailed record keeping.
  • Proven experience, awareness and understanding with working within the ISO 17025 Quality Management System (QMS) or equivalent and a robust understanding of the requirements that can be transferred to a variety of QMS.
  • Experience of developing, implementing, maintaining and reviewing systems and services to ensure delivery of professional excellence, and working with stakeholders to develop suggestions for improvements.
  • Experience in leading internal audits and be able to identify issues and provide constructive feedback to auditees as to how non-conformities can be resolved.
  • Ability to review and interpret complex scientific data against requirements of a Quality Management System (QMS) and draw conclusions regarding compliance to requirements, test methods and specifications.

Person Specification:

Method of assessment: A=Application, T=Test, I=Interview, P=Presentation

Behaviour Criteria:

  • Seeing the Big Picture (A, I)
  • Leadership (A, I)
  • Changing and Improving (A, I)
  • Working Together (A, I)

Experience Criteria:

  • Proven experience, awareness and understanding with working within the ISO 17025 Quality Management System (QMS) or equivalent and a robust understanding of the requirements that can be transferred to a variety of QMS (A, I, P)
  • Experience in leading internal audits and be able to identify issues and provide constructive feedback to auditees as to how non-conformities can be resolved (A, I)
  • Experience of developing, implementing, maintaining and reviewing systems, services and processes to ensure delivery of professional excellence, and working with stakeholders to develop suggestions for improvements (A, I, P)

Technical Criteria:

  • BSc in a relevant biological discipline e.g. biochemistry, microbiology, immunology, molecular biology and experience of detailed record keeping (A, I)
  • In-depth practical experience of a broad range of relevant biological laboratory techniques undertaken within a Quality Management System and reviewing and interpreting complex scientific data against requirements and specifications (A, I)

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. 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. Presentation, to be prepared as part of your interview, with further information being supplied when you reach this stage. 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 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.

Use of AI in Job Applications: Artificial Intelligence can be a useful tool to support your application, however, all examples and statements provided must be truthful, factually accurate and taken directly from your own experience. Where plagiarism has been identified (presenting the ideas and experiences of others, or generated by artificial intelligence, as your own) applications may be withdrawn and internal candidates may be subject to disciplinary action. Please see our candidate guidance for more information on appropriate and inappropriate use.

If you require any disability related adjustments at any point during the process, please contact careers@mhra.gov.uk as soon as possible.

Closing date: 4th August 2026

Shortlisting date: from 13th August 2026

Interview date: from 24th August 2026

If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.uk

Candidates will be subject to UK immigration requirements as well as Civil Service nationality rules. Further information on whether you are able to apply is available here.

Successful candidates must pass a disclosure and barring security check as well as animal rights and pro-life activism checks. People working with government assets must complete basic personnel security standard checks.

Certain roles within the MHRA will require post holders to have vaccinations, and in some circumstances, routine health surveillance. These roles include:

  • Laboratory-based roles working directly with known pathogens
  • Maintenance roles, particularly those required to work in laboratory settings
  • Roles that involve visiting other establishments where vaccination is required
  • Roles required to travel overseas where specific vaccination may be required.

Applicants who are successful at interview will be, as part of pre-employment screening subject to a check on the Internal Fraud Database (IFD). This check will provide information about employees who have been dismissed for fraud or dishonesty offences. This check also applies to employees who resign or otherwise leave before being dismissed for fraud or dishonesty had their employment continued. Any applicant’s details held on the IFD will be refused employment. A candidate is not eligible to apply for a role within the Civil Service if the application is made within a 5 year period following a dismissal for carrying out internal fraud against government.

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.

Individuals appointed on level transfer will retain their existing salary and are responsible for ensuring they fully understand the financial implications of any potential move and the impact (if any) on their terms. If an individual is in any doubt, they should seek clarification before accepting a job offer.

Staff joining on promotion will receive up to a 10% increase of their current basic salary, or the pay band minimum, whichever is the greater. The individual will not retain any allowances paid by the former department/Agency, unless there are special circumstances, such as a reserved right to those allowances on transfer.

Successful candidates may be subject to annual Occupational Health reviews dependent on role requirements. If you have any queries, please contact careers@mhra.gov.uk.

In accordance with the Civil Service Commissioners’ Recruitment Principles our recruitment and selection processes are underpinned by the requirement of selection for appointment on the basis of merit by a fair and open competition. If you feel your application has not been treated in accordance with the Recruitment Principles and you wish to make a complaint, in the first instance, you should contact the MHRA Recruitment Team at careers@mhra.gov.uk. If you are not satisfied with the response you receive, you can contact the Civil Service Commission at: civilservicecommission.independent.gov.uk info@csc.gov.uk Civil Service Commission Room G/8 1 Horse Guards Road London SW1A 2HQ

Quality Lead employer: Medicines and Healthcare Products Regulatory Agency

The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a strong commitment to employee growth, the agency provides opportunities for professional development and collaboration with leading experts in healthcare and research. The hybrid working model promotes a healthy work-life balance, while the agency's focus on innovation and public health ensures that employees contribute to meaningful projects that enhance the well-being of millions.

Medicines and Healthcare Products Regulatory Agency

Contact Details:

Medicines and Healthcare Products Regulatory Agency Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Lead

Get Involved in Local Research Communities

Tap into local biotechnology meetups and research forums. These are great places to mingle with industry professionals, share your passion, and even discover unadvertised job openings. It's all about getting your face known in the field!

Leverage University Alumni Networks

If you're a recent grad, don’t underestimate the power of your university’s alumni network! Reach out to alumni working in biotechnology to gather tips about job openings at companies like Medicines and Healthcare Products Regulatory Agency. You'd be surprised how willing people are to help out a fellow grad!

Show Off Your Projects

Curate a portfolio showcasing any research projects or internships you've completed in biotechnology. This tangible evidence of your skills can really impress employers when you chat with them at networking events or interviews. It's about making that killer first impression!

Stay Up-to-Date with Industry Trends

Biotech is a fast-paced field, so keeping yourself updated with the latest advancements is crucial. Attend industry conferences, webinars, or workshops to broaden your knowledge and meet potential employers. Plus, it’ll give you fantastic talking points for your interviews at places like Medicines and Healthcare Products Regulatory Agency!

We think you need these skills to ace Quality Lead

ISO 17025
Quality Management Systems (QMS)
Auditing Skills
Problem-Solving Skills
Training and Development
Stakeholder Engagement
Data Interpretation

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Medicines and Healthcare Products Regulatory Agency that you have the hands-on skills they need.

Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at Medicines and Healthcare Products Regulatory Agency.

Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Medicines and Healthcare Products Regulatory Agency does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.

How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Medicines and Healthcare Products Regulatory Agency. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.

Show Your Teamwork Skills

Biotech often involves collaboration across multiple disciplines. Be ready to share stories that highlight your teamwork and communication skills, especially in research projects. Think about working with different teams at university or any internships – this is where you can show how well you fit into Medicines and Healthcare Products Regulatory Agency's culture.

Research Recent Biotech Innovations

Stay updated on the latest trends and breakthroughs in biotechnology. Knowing what's happening in the field can help you engage in more meaningful discussions during your interview. Bring up recent articles or advancements that excite you, especially those related to the work being done at Medicines and Healthcare Products Regulatory Agency. This shows your passion for the industry!