156 Clinical Laboratory Scientists jobs in the United Kingdom

Looking for a rewarding career by the coast? Join our friendly and forward-thinking Chemistry team at University Hospitals Sussex NHS Foundation Trust. Based mainly at Worthing Hospital, with support to Chichester's St Richard's site, you'll enjoy the work-life balance of living in two of the South East's most desirable coastal towns. Worthing offers a vibrant coastal lifestyle, with a wide choice of cafés, restaurants, and shops, all set against the backdrop of a beautiful beach. The seafront and surrounding countryside encourage an active, healthy work-life balance – perfect for those who enjoy running, cycling, water sports, or simply unwinding by the sea.

An exciting opportunity has arisen for a Senior Medical Laboratory Assistant post in chemistry.

We offer a supportive environment, excellent development opportunities, and access to well-equipped labs.

The laboratory is implementing a 24/7 shift system during 2025/26 which the post holder will be expected to fully participate in (including nights, weekends and bank holidays) subject to competency assessment.

Help shape the future of diagnostics at UHSussex — where innovation, learning, and community thrive.

To assist other team members in the receipt, registration, preparation and analysis of pathological specimens for Biochemistry. To assist in the administration of the department as directed.

At UHSussex (UHSx), diversity is our strength, & we want you to feel included to help us always put the Patient First. Your uniqueness & experiences will be part of our creative and innovative community where everyone is encouraged to succeed. We have a range of Staff Networks to help break down barriers, & can offer a buddy to help new members settle in. We're proud to be a Disability Confident Employer (Level 2) & a Veteran Aware Trust.

We treat our patients & staff with the same compassion & empathy we expect for ourselves. We're here for them when they need us, and we go above & beyond to meet their needs. This can be seen in our candidate information pack & wellbeing programme, for staff which is extensive & designed to support you when you need it, including where possible, flexible working to support work life balance - because we know that to look after others we must first look after ourselves.

As a university trust and a leader in healthcare research, we value learning, teaching & training so that we can be the best that we can be. From the moment you start with us & throughout your career we will help you to grow & develop. We hope that in choosing UHSx you are choosing a long & happy career where you will be able to see the difference you make & feel valued for all that you do.

We look forward to receiving your application & the start of your journey with UHSx.

Candidate Information Pack:

Once trained you will be expected to;

• To work in accordance with Departmental policy and Standard Operating procedures.
• To receive, distribute and prepare patient specimens for diagnostic laboratory testing.
• Process and store samples for clinical trials.
• Assist with the daily maintenance and running of departmental analysers including loading and unloading.
• Undertake competency assessment appropriate to work area.
• Clean equipment for use by others and inform supervisor when stock levels are low.
• Use accurate pipetting skills.
• Be familiar with routine use of laboratory's computer systems.
• Use QPulse Quality Management Software
• To perform all duties with reference to Standard Operating procedures and propose changes to SOPs when required.
• To comply with Departmental and Trust information governance standards at all times.
• To be familiar with the laboratory's Quality Policy and Quality Manual and to ensure that a high standard of work is maintained at all times.
• To contribute to developing the service to ensure that delivery is safe, effective, cost effective and follows best practice.
• Ensure confidentiality at all times. Employees of the trust must not disclose any information obtained during the course of employment regarding patients or staff except to authorised bodies or individuals acting in an official capacity.
• Be aware of and adhere to the Trust's infection control policy.

Please see job description & person specs for full details

• Perform a wide range of microbiological tests on patient samples, including culture, identification, and susceptibility testing.
• Operate and maintain sophisticated laboratory equipment, such as automated culture systems, mass spectrometers, and PCR platforms.
• Interpret and report test results accurately and efficiently, often under pressure.
• Implement and monitor quality assurance procedures to ensure the highest standards of laboratory practice.
• Troubleshoot technical issues with instrumentation and methodologies, escalating complex problems as needed.
• Participate in the validation of new laboratory tests and technologies.
• Assist in the training and supervision of junior laboratory staff and students.
• Maintain detailed and accurate laboratory records in compliance with regulatory requirements.
• Contribute to the development and implementation of laboratory policies and procedures.
• Ensure a safe working environment by adhering to health and safety regulations.
• Liaise with clinicians and other healthcare professionals regarding test results and interpretation.
• Participate in continuing professional development to stay current with advancements in microbiology.
• Contribute to departmental audits and performance improvement initiatives.
• Manage laboratory inventory and reagents, ensuring adequate stock levels.

• A Bachelor's or Master's degree in Microbiology, Biomedical Science, or a related field.
• HCPC registration (or eligibility to register).
• Significant post-qualification experience working as a Medical Laboratory Scientist in a clinical microbiology setting.
• Demonstrated expertise in diagnostic microbiology techniques, including bacteriology, virology, mycology, and parasitology.
• Proficiency in operating and maintaining a variety of laboratory instruments.
• Strong understanding of quality control, accreditation standards (e.g., UKAS), and health and safety legislation.
• Excellent analytical and problem-solving skills.
• Meticulous attention to detail and a commitment to accuracy.
• Effective communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Experience in staff supervision or training is advantageous.
• Familiarity with laboratory information management systems (LIMS).

UL Solutions' Built Environment department in Telford is hiring We're looking for a Laboratory Assistant who will be focused on assisting our Lab Technicians and Engineers during testing of a range of fenestration products (doors and windows. This will include setting up test rigs, assisting with the testing process and reporting post-testing.

Largely working in indoor environment (mainly physical work, but desk-based tasks required such as filling in excel/word templates as well as completing training).

This is a great opportunity for someone who's seeking variety in their role, as at UL Solutions, no two days are the same You also have a genuine opportunity to grow your career here, in a small, close-knit team with good people. The aim for this role would be to progress within our engineering function, from Laboratory Technician to Engineering Technician.

• Assists in manual and mechanical testing of door hardware/furniture. Sets up and prepares test samples, materials and equipment.
• Diligently follows test procedures, standards and requirements.
• Operates designated machines, special laboratory equipment and tools as directed.
• Routinely carries out maintenance to test rigs, and test equipment.
• Receives instructions from and reports to supervisor and personnel in engineering and laboratory operations as needed. Assists in recording observed data on appropriate UL forms.
• May support in preparation of instructions for test methods and procedures
• May support in the preparation of test reports.
• Manual and physical work included.
• Examines test chambers/samples, reads drawings and measuring instruments.

• Develops knowledge of applicable test requirements and operational instructions.

• Ability to work manually, building rigs, new jigs, set up of equipment.

• Ability to use hand/power tools to a high standard.
• Ability to interpret technical information and understanding technical plans and drawings would be beneficial.
• Ability to work well within the Microsoft office suite.
• Good attention to detail and ability to follow procedures.
• Good team player with ability to work individually as well.
• Enthusiasm to learn and good interpersonal skills.
• Positive attitude and good work ethic.
• FLT, IPAF, Harness Awareness/User and CSCS would be beneficial.

A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers' product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers' products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.

Our buildings don't just shape our skylines — they provide the backdrop to our lives. And knowing they're safe matters. We've been helping to create safer structures since 1894, combining our expertise with innovative new technologies to help make sure both people and property are secure. As more people have to deal with extreme weather, we're on hand to test products and building materials to increasingly rigorous standards. Whether we're simulating tornadoes or testing smoke alarms, the work we do on our team is used in buildings around the world to — quite literally — help save lives. Join our team and build your skills, build innovative solutions and help build a safer world.

• Perform advanced analytical testing on environmental samples (e.g., water, soil, air) using various laboratory techniques and instrumentation.
• Prepare samples and reagents, ensuring accuracy and consistency.
• Operate, calibrate, and maintain laboratory equipment such as (mention specific equipment relevant to the field, e.g., GC-MS, ICP-OES, spectrophotometers).
• Implement and adhere to quality assurance and quality control (QA/QC) protocols to ensure data integrity.
• Interpret and analyse test results, documenting findings accurately in laboratory reports.
• Troubleshoot technical issues and identify solutions to maintain workflow efficiency.
• Manage laboratory consumables and inventory.
• Assist in the development and validation of new testing methods.
• Ensure compliance with health, safety, and environmental regulations within the laboratory.
• Potentially supervise and train junior laboratory staff.

• HND or BSc in a relevant scientific discipline (e.g., Chemistry, Environmental Science, Biology).
• Proven experience working in a laboratory environment, with a focus on environmental testing.
• Proficiency with standard laboratory techniques and analytical instrumentation.
• Strong understanding of QA/QC procedures and data interpretation.
• Excellent organisational skills and meticulous attention to detail.
• Ability to work independently and as part of a team.
• Good written and verbal communication skills.
• Knowledge of ISO 17025 or similar quality standards is desirable.

Job Description

We’re hiring a Laboratory Scientist to join a cutting-edge biotech firm conducting breakthrough research in gene therapies and molecular diagnostics. You’ll perform hands-on experiments, analyse data, and contribute to IP development in a dynamic R&D lab setting.

Job Responsibilities

Required Skills

Desired Skills

Benefits

Medical Writer | Clinical Scientist | CER Writer

If you want a position where you're not lost in a 10 layer org chart for progression and you are surrounded by experienced people to learn and advance in your career. This is it.

Working with a well recognised Medical Device manufacturer as a Clinical Scientist, you are here to make sure the science holds up, the data says what it needs to say and that patients are genuinely better off for using the medical devices this company bring to market.

You’ll join a small but experienced Clinical Affairs team supporting highly regulated Class II & III devices, working to review all clinical and technical documentation to close out clinical gaps so the products remain safe and compliant.

If you’ve written or contributed to Clinical Evaluation Reports (CERs), understand EU MDR expectations, this could be the step you’ve been looking for.

Your core focus will be writing and maintaining Clinical Evaluation Reports (CERs) using real world data and clinical feedback.

You’ll:

• Analyse post-market data (e.g., complaints, feedback, literature, internal reports)
• Summarise performance and safety outcomes against MDR criteria
• Identify clinical data gaps and support study planning
• Contribute to risk assessments alongside R&D and Regulatory Affairs
• Attend relevant conferences and learn from clinical users directly

Must-haves:

• 1–2 years in the medical device industry
• Practical experience writing or contributing to CERs
• Strong analytical and written communication skills
• Comfort working with data and basic statistical tools (e.g., Excel, SPSS, R)

The company offer flexible working (2 days remote) and half day Fridays.

Not only that, they want to create opportunities for their staff to progress.

The last person hired here went from grad to senior specialist within 3 years.

If this sounds of interest, then please apply and I will be in touch.

COMPANY OVERVIEW

AIRNA is a biotechnology company with a mission to be the leading RNA editing company delivering precision therapies to patients with rare and common diseases.

AIRNA is harnessing advances in genetics to develop transformative RNA-editing medicines that improve human health. Our proprietary platform is based on groundbreaking research by pioneers of the field and company co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University) and enables optimal potency, safety, and delivery. AIRNA is advancing a robust pipeline of therapeutic candidates that are designed to provide functional cures for severe or chronic diseases by repairing harmful genetic variants or introducing beneficial variants promote optimal health.

AIRNA has raised $245 million in financing from a world-class syndicate of investors including Arch Venture Partners, Forbion, Venrock Healthcare Capital Partners, RTW Investments, Nextech Invest, and ND Capital. We value teamwork, resilience, excellence, human, and health, and have a diverse team at both our headquarters in Cambridge, MA and our research operations in Tübingen, Germany.

JOB OVERVIEW

The Clinical Scientist supports the design, execution, and analysis of clinical trials that are part of AIRNA’s RNA editing platform. Working closely with Clinical Development, Clinical Operations, and external clinical trial site staff, the clinical scientist will ensure scientific integrity and operational excellence in AIRNA’s clinical trials.

RESPONSIBILITIES

Clinical Trial Design & Protocol Development

• Assist in or lead the design of clinical study protocols and amendments
• Write or contribute to study-related documents (e.g., IB, informed consent forms, CRFs, recruitment materials)

Study Execution Support

• Provide scientific and clinical input during trial conduct
• Monitor data for consistency, completeness, and potential safety/efficacy signals
• Collaborate with CROs, sites, and internal teams to resolve study-related issues
• Build relationships with sites including PIs and clinical trial site staff, supporting their start up activities and patient recruitment activities

Data Analysis & Interpretation

• Review clinical trial data in collaboration with data management and biostatistics
• Interpret data in the context of the disease, target, and competitive landscape
• Contribute to clinical study reports and documentation for regulatory submissions

Cross-functional Collaboration

• Work closely with Clinical Operations, Medical Monitors, Pharmacovigilance, and Regulatory Affairs
• Participate in clinical development plan creation and updates
• Present study results and strategy to internal stakeholders and internal governance bodies

Regulatory & Safety Input

• Support preparation of INDs, NDAs, CTAs and other regulatory documents
• Provide input into safety review processes and risk-benefit assessments

QUALIFICATIONS

Education:

• Advanced degree in life sciences or health discipline (PhD, PharmD, MD, or MS with relevant experience)

Experience:

• 2–6+ years of industry experience in clinical development and/or clinical operations

Skills:

• Strong knowledge of ICH GCP and clinical trial methodology
• Ability to critically evaluate scientific data and literature
• Strong communication skills (verbal and written)
• Ability to manage multiple priorities and collaborate across functions

Preferred Attributes:

• Experience in rare disease, including pulmonary/hepatic diseases
• Familiarity with working with and supporting clinical trial sites for study start-up and recruitment
• Working knowledge of clinical trial site monitoring
• Ability to travel to clinical trial sites and build relationships with PIs and clinical trial site staff

LOCATION

• This is a remote position that will require travel to sites. A candidate based in Europe/UK is preferred.