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Biomedical Scientist jobs in England

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    • You will report directly to the Laboratory Manager and play a pivotal role in driving quality, consistency, and innovation across all aspects of blood science…
    • The candidate must be competent and confident in interpreting and reporting all aspects of microbiology analysis.
    • Be able to problem solve when necessary.
    • Perform and report a range of routine blood science tests including haematology, biochemistry, and coagulation assays.
    • This role is for a scientist who thrives in the lab and is driven to solve complex analytical challenges.
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    • The position is within a NHS Hospital in Manchester amongst a strong team, developing new techniques and working to maintain the highest standards within the…
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    • Work in collaborating centers abroad/with visiting scientists as required.
    • Flexible working, Full-time, Job share, Part-time.
    • Participate in RIPL on-call team.
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    • Up to £45,000-£50,000 depending on experience.
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Job Post Details

Senior Biomedical Scientist - job post

Clinilabs
4.0 out of 5 stars
41 Foley Street, London W1W
From £50,000 a year - Full-time

Job details

Pay

  • From £50,000 a year

Job type

  • Full-time

Location

41 Foley Street, London W1W

Benefits

Pulled from the full job description

  • Employee discount
  • Private medical insurance

Full job description

The Opportunity

We are seeking an experienced, highly motivated Senior Biomedical Scientist to join our young multi-disciplinary Blood Sciences laboratory at a senior level. This is a rare chance to shape a laboratory from the early stages, working at the intersection of clinical excellence and operational leadership.

You will report directly to the Laboratory Manager and play a pivotal role in driving quality, consistency, and innovation across all aspects of blood science testing.

Key Responsibilities

Day-to-Day Leadership

  • Manage and coordinate the daily technical activities of the laboratory team
  • Act as the senior technical point of contact for complex or escalated cases
  • Support, mentor, and performance-manage junior BMS staff
  • Organise and chair regular team meetings

Sample & Analytical Management

  • Oversee the accessioning, processing, storage, and chain of custody of all samples
  • Manage the full testing workflow: analysis, result validation, and quality improvement
  • Ensure timely and accurate generation and authorisation of clinical reports

Quality & Compliance

  • Maintain and enforce up-to-date SOPs across all laboratory functions
  • Manage internal and external quality assurance programmes (IQA/EQA)
  • Ensure full UKAS/ISO 15189 compliance and readiness at all times
  • Oversee clinical and health & safety training and records

Analyser & Inventory Management

  • Manage QC, calibration, maintenance, and troubleshooting of all analysers
  • Maintain adequate and cost-effective stock of consumables and reagents
  • Liaise with suppliers and engineers as required

Requirements

Essential

  • Ambitious and hungry individual looking to drive impact and learn, operating within a small agile team
  • HCPC registration as a Biomedical Scientist (BMS)
  • Demonstrable experience at Senior BMS level or equivalent (Band 7 or above)
  • In-depth knowledge of blood sciences: haematology, biochemistry, coagulation, immunology and microbiology
  • Highly organised and structured mind with strong critical thinking skills and ability to analyse outcomes scientifically
  • Strong understanding of laboratory best practices, QHSE systems, and regulatory frameworks (UKAS, ISO 15189, CPA)
  • Proficiency with LIMS platforms and MS Office (particularly Excel for data management and QC trending) and AI tools
  • Confident communicator with the ability to engage clinicians, patients, and colleagues at all levels
  • Ability to work autonomously, prioritise effectively under pressure, and lead a team

Desirable

  • Experience with analysers from Werfen, Beckman Coulter, Sebia, Cepheid, or Alifax.
  • Experience in a private pathology or independent laboratory setting.
  • Familiarity with LIS/middleware integration and digital pathology workflows.
  • Track record of contributing to service development, SOP authorship, or quality improvement initiatives.

About Clinilabs

Clinilabs is a multi-disciplinary pathology laboratory in the heart of London, dedicated to providing the highest-quality, patient-centred diagnostic services. Led by some of the UK's most experienced pathologists - with over 30 years serving London's top medical institutions - we partner with the city's leading private healthcare providers across all diagnostic disciplines.

We are building something exciting: a fast-paced, high-growth environment where ambition is recognised and rewarded. Clinilabs operates on merit, so your compensation reflects your expertise and impact. We actively encourage new thinking and continuous improvement, and the people who drive that are the people who progress here.

What We Offer

+ Competitive salary commensurate with experience, plus performance-based incentives

+ Core business days, Monday-Friday and some Saturdays (pre arranged shift patterns)

+ True meritocracy - your growth is limited only by your performance and ambition

+ Beautiful 2,000 sq ft workspace across two floors in the heart of Oxford Circus

How to Apply

If you are a motivated and experienced BMS professional ready to take the next step in a growing, ambitious laboratory - we would love to hear from you.

Please send your CV and a brief cover letter to:

careers@clinilabs.co.uk

Applications are reviewed on a rolling basis but we are looking to hire ASAP - early applications are strongly encouraged.

Clinilabs is an equal opportunities employer

Job Type: Full-time

Pay: From £50,000.00 per year

Benefits:

  • Employee discount

Application question(s):

  • Are you HCPC-registered as a Biomedical Scientist?
  • What band/level are you currently working at, and how long have you been at that level?
  • Have you had hands-on responsibility for managing an EQA scheme? If so, which schemes (e.g. NEQAS, RIQAS) and for which disciplines?
  • Walk us through a time an analyser or method failed QC. What steps did you take to investigate, document, and resolve it before releasing results?
  • Describe your experience with IQC - have you been responsible for setting Westgard rules, reviewing Levey-Jennings charts, and taking corrective action on QC failures?

Licence/Certification:

  • HCPC (required)

Work authorisation:

  • United Kingdom (required)

Work Location: In person

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